Pharmaceutical Inorganic chemistry UNIT-V Radiopharmaceutical.pptx
Isotopes Types of decay
Alpha rays, which could barely penetrate a piece of paper
Beta rays, which could penetrate 3 mm of aluminium
Gamma rays, which could penetrate several centimetres of lead
Units of Radioactivity:
Measurement of Radioactivity
The measurement of nuclear radiation and detection is an important aspect in the identification of type of radiations (, , ) and to assay the radionuclide emitting the radiation, suitable detectors are required. The radiations are identified on the basis of their properties.
e.g. Ionization effect is measured in Ionization Chamber, Proportional Counter and Geiger Muller Counter.
The scintillation effect of radiation is measured using scintillation detector and the photographic effect is measured by Autoradiography.
Gas Filled Detectors:
Ionization Chamber:
Proportional Counters:
Geiger-Muller Counter
Properties of α, β, γ radiations
Half –life of Radioelement
Sodium Iodide (I131)
Handling and Storage of Radioactive Material:
Storage of Radioactive Substances –
Precautions For Handling Radioactive Substances
Labelling of Radioactive Substances
Pharmaceutical Application Of Radioactive Substances
Acids, Bases And Buffers Pharmaceutical Inorganic chemistry UNIT-II (Part-I)
Acids, Bases are defined by Four main theories,
1.Traditional theory / concept
2.Arrhenius theory
3.Bronsted and Lowry theory
4.Lewis theory
Importance of acids and bases in pharmacy
Buffers: Buffer action
Buffer capacity Buffers system
Types of Buffers : Generally buffers are of two types:
1. Acidic buffers
2. Basic buffers
There are some other buffer system:
3. Two salts acts as acid-base pair. Ex- Potassium hydrogen phosphate and potassium dihydrogen phosphate.
4. Amphoteric electrolyte. Ex- Solution of glycine.
5. Solution of strong acid and solution of strong base. Ex- Strong HCl with KCl Mechanism of Buffer action: Mechanism of Action of acidic buffers: Buffer equation-Henderson-Hasselbalch equation:
Standard Buffer Solutions Preparation of Buffer Solutions: Buffers in pharmaceutical systems or Application of buffer: Stability of buffers Buffered isotonic solution Types of Buffer Isotonic solution
1. Isotonic Solutions:
2. Hypertonic Solutions:
3. Hypotonic Solution:
Measurement of Tonicity: 1. Hemolytic method: 2. Cryoscopic method or depression of freezing point:
Methods of adjusting the tonicity:
Class I methods:
In this type, sodium chloride or other substances are added to the solution in sufficient quantity to make it isotonic. Then the preparation is brought to its final volume withan isotonic or a buffered isotonic diluting solution.
These methods are of two types:
Cryoscopic method
Sodium chloride equivalent method.
Class II methods:
In this type, water is added in sufficient quantity make the preparation isotonic. Then the preparation is brought to its volume with an isotonic or a buffered isotonic diluting solution.
These methods are of two types:
White-Vincent method
Sprowls method.
Major extra and intracellular electrolytes. Pharmaceutical Inorganic chemistr...Ms. Pooja Bhandare
Major extra and intracellular electrolytes. Pharmaceutical Inorganic chemistry UNIT-II (Part-II)
Electrolyte: Intracellular fluid
Interstitial fluid
Plasma (Vascular fluid)
Anionic electrolytes- HCO₃⁻, Cl⁻, SO₄²⁻, HPO₄²⁻
Cationic electrolytes- Na⁺, K⁺, Ca²⁺, Mg²⁺
Concentration of important Electrolytes:
Electrolytes used in the replacement therapy: Sodium
chloride*, Potassium chloride, Calcium gluconate* and Oral Rehydration Salt
(ORS), Physiological acid base balance.
Pharmacopoeias,Sources of Impurities in Medicinal agents and Limit testssaimuniswetha1
Today's Topic Pharmacopoeias, Sources of Impurities in Medicinal agents and Limit tests for Chlorides, Sulphates, Heavy Metals, Lead, Iron in Pharmaceutical Analysis subject for B.pharmacy 1st year as per JNTUA Syllabus...
Acids, Bases And Buffers Pharmaceutical Inorganic chemistry UNIT-II (Part-I)
Acids, Bases are defined by Four main theories,
1.Traditional theory / concept
2.Arrhenius theory
3.Bronsted and Lowry theory
4.Lewis theory
Importance of acids and bases in pharmacy
Buffers: Buffer action
Buffer capacity Buffers system
Types of Buffers : Generally buffers are of two types:
1. Acidic buffers
2. Basic buffers
There are some other buffer system:
3. Two salts acts as acid-base pair. Ex- Potassium hydrogen phosphate and potassium dihydrogen phosphate.
4. Amphoteric electrolyte. Ex- Solution of glycine.
5. Solution of strong acid and solution of strong base. Ex- Strong HCl with KCl Mechanism of Buffer action: Mechanism of Action of acidic buffers: Buffer equation-Henderson-Hasselbalch equation:
Standard Buffer Solutions Preparation of Buffer Solutions: Buffers in pharmaceutical systems or Application of buffer: Stability of buffers Buffered isotonic solution Types of Buffer Isotonic solution
1. Isotonic Solutions:
2. Hypertonic Solutions:
3. Hypotonic Solution:
Measurement of Tonicity: 1. Hemolytic method: 2. Cryoscopic method or depression of freezing point:
Methods of adjusting the tonicity:
Class I methods:
In this type, sodium chloride or other substances are added to the solution in sufficient quantity to make it isotonic. Then the preparation is brought to its final volume withan isotonic or a buffered isotonic diluting solution.
These methods are of two types:
Cryoscopic method
Sodium chloride equivalent method.
Class II methods:
In this type, water is added in sufficient quantity make the preparation isotonic. Then the preparation is brought to its volume with an isotonic or a buffered isotonic diluting solution.
These methods are of two types:
White-Vincent method
Sprowls method.
Major extra and intracellular electrolytes. Pharmaceutical Inorganic chemistr...Ms. Pooja Bhandare
Major extra and intracellular electrolytes. Pharmaceutical Inorganic chemistry UNIT-II (Part-II)
Electrolyte: Intracellular fluid
Interstitial fluid
Plasma (Vascular fluid)
Anionic electrolytes- HCO₃⁻, Cl⁻, SO₄²⁻, HPO₄²⁻
Cationic electrolytes- Na⁺, K⁺, Ca²⁺, Mg²⁺
Concentration of important Electrolytes:
Electrolytes used in the replacement therapy: Sodium
chloride*, Potassium chloride, Calcium gluconate* and Oral Rehydration Salt
(ORS), Physiological acid base balance.
Pharmacopoeias,Sources of Impurities in Medicinal agents and Limit testssaimuniswetha1
Today's Topic Pharmacopoeias, Sources of Impurities in Medicinal agents and Limit tests for Chlorides, Sulphates, Heavy Metals, Lead, Iron in Pharmaceutical Analysis subject for B.pharmacy 1st year as per JNTUA Syllabus...
This slide contains the details from topic, "Dental Product", B.Pharm 1st Semester, Pharmaceutical Inorganic Chemistry.
Dental Product
Desensitizing Agent
Dental Caries
Dentifrices
Role of Fluoride
Neutralization curves in acid base analytical titrations, indicators.nehla313
Neutralization curves in acid base analytical titrations, indicators,
strong acid strong base
weak acid strong bse
strong acid weak base
weak acid and weak base
This is chapter No 3 of Pharmaceutical Chemistry - I for Diploma in Pharmacy (D. Pharmacy) Details notes for Diploma in Pharmacy (D.Pharmacy) Students.
This slide contains the details from topic, "Dental Product", B.Pharm 1st Semester, Pharmaceutical Inorganic Chemistry.
Dental Product
Desensitizing Agent
Dental Caries
Dentifrices
Role of Fluoride
Neutralization curves in acid base analytical titrations, indicators.nehla313
Neutralization curves in acid base analytical titrations, indicators,
strong acid strong base
weak acid strong bse
strong acid weak base
weak acid and weak base
This is chapter No 3 of Pharmaceutical Chemistry - I for Diploma in Pharmacy (D. Pharmacy) Details notes for Diploma in Pharmacy (D.Pharmacy) Students.
Complete detail about the Radiopharmaceutical, General Introduction, Radioactive substance, Radioactive rays like alpha, beta and gamma rays. All the Measurement method to determine the radioactivity of any element and widely used instrument Geiger Muller Counter. And some Radiopharmaceutical product used in many diagnosis , treatment such like sodium iodide solution & capsule, Rose Bengal I 131 and Application of Radiopharmaceuticals.
An isotope is one of two or more atoms having the same atomic number but different mass numbers.
Unstable isotopes are called Radioisotopes.
uses of radioisotopes are many which are discussed in this slide.
gm counter .working principle of gm counter, construction, advantage and disadvantage of gm counter.
Scintillation counter, its history, solid and liquid scintillation, scintillation cocktail, photomultiplier tube, advantage, and disadvantage.
Pharmaceuticals: In some pharmaceutical manufacturing processes, minute quantities of a catalyst used in the process (usually a metal) are sometimes present in the final product. By using AAS the amount of catalyst present can be determined.
Atomic absorption spectroscopy (AAS) and atomic emission spectroscopy (AES) is a spectro analytical procedure for the quantitative determination of chemical elements by free atoms in the gaseous state.
Atomic absorption spectroscopy is based on absorption of light by free metallic ions.
In analytical chemistry the technique is used for determining the concentration of a particular element (the analyte) in a sample to be analyzed. AAS can be used to determine over 70 different elements in solution, or directly in solid samples via electrothermal vaporization
Atomic absorption spectrometry (AAS) is an analytical technique that measures the concentrations of elements.
Atomic absorption is so sensitive that it can measure down to parts per billion of a gram (µg dm–3 ) in a sample.
The technique makes use of the wavelengths of light specifically absorbed by an element. They correspond to the energies needed to promote electrons from one energy level to another, higher, energy level.
Atomic absorption spectrometry has many uses in different areas of chemistry.
Clinical analysis : Analysing metals in biological fluids such as blood and urine.
Environmental analysis: Monitoring our environment – eg finding out the levels of various elements in rivers, seawater, drinking water, air, petrol and drinks such as wine, beer and fruit drinks.
The technique makes use of the atomic absorption spectrum of a sample in order to assess the concentration of specific analytes within it. It requires standards with known analyte content to establish the relation between the measured absorbance and the analyte concentration and relies therefore on the [Beer–Lambert law].
The electrons within an atom exist at various energy levels. When the atom is exposed to its own unique wavelength, it can absorb the energy (photons) and electrons move from a ground state to excited states.
The radiant energy absorbed by the electrons is directly related to the transition that occurs during this process.
Furthermore, since the electronic structure of every element is unique, the radiation absorbed represents a unique property of each individual element and it can be measured.
An atomic absorption spectrometer uses these basic principles and applies them in practical quantitative analysis
A typical atomic absorption spectrometer consists of four main components:
Atomization
Light source,
Atomization system,
Monochromator &
Detection system
Atomization can be carried out either by a flame or furnace.
Heat energy is utilized in atomic absorption spectroscopy to convert metallic elements to atomic dissociated vapor.
The temperature should be controlled very carefully for the conversion of atomic vapor.
At too high temperatures, atoms
Different Types of Radioactive Counters or detectors used in analyzing low or high penetrating power radiation or particles are explained briefly with their advantages and disadvantages.
Medha Thakur (M.Sc Chemistry)
Similar to Pharmaceutical Inorganic chemistry UNIT-V Radiopharmaceutical.pptx (20)
Limt test Pharmaceutical Inorganic chemistry UNIT-I (Part-III) Limit Test.
Limit tests:- Factors affecting limit tests:
Specificity of the tests
Sensitivity
Control of personal errors (Analyst errors)
Test in which there is no visible reaction
Comparison methods
Quantitative determination
Limit test for Chloride: Principle, Procedure, observation and result.
Limit test for Sulphate: Principle, Procedure, observation and result
Limit test for Iron: Principle, Procedure, observation and result.
Limit test for Heavy metal: Principle, Procedure, observation and result.
Limit test for Lead: Principle, Procedure, observation and result.
Limit test for Arsenic: Principle, Gutzet test Procedure, detail in Gutzet Apparatus. observation and result.
Modifies Limit test for Chloride: Principle, Procedure, observation and result.
Modified Limit test for sulphate: Principle, Procedure, observation and result.
Types and Sources of impurities.pptx Pharmaceutical Inorganic chemistry UNIT-...Ms. Pooja Bhandare
Types and Sources of impurities. Pharmaceutical Inorganic chemistry UNIT-I (Part-II) Impurities:
Impure Chemical Compound
Pure Chemical Compound.
Types of impurities: Organic Impurity, Inorganic impurity, Residual solvent, Sources of Impurities in Pharmaceuticals
The different sources of impurities in pharmaceuticals are listed below:
Raw material used in manufacture
Reagents used in manufacturing process
Method/ process used in manufacture or method of manufacturing
Chemical processes used in the manufacture
Atmospheric contamination during the manufacturing process
Intermediate products in the manufacturing process
Defects in the manufacturing process
Manufacturing hazards
Inadequate Storage conditions
Decomposition of the product during storage
Accidental substitution or deliberate adulteration with spurious or useless materials.
Test for purity: Pharmacopoeia prescribes the “Test for purity” for pharmaceutical substances to check their freedom from undesirable impurities.
Pharmacopoeia will decide and fix the limit of tolerance for these impurities.
For certain common impurities for which pharmacopoeia prescribes the test of purity are:
Colour, odour, taste
Physicochemical constants (Iodine value, saponification value, melting point, refractive index etc.)
Acidity, alkalinity, pH
Humidity (Estimation of moisture)
Cations and anions
Insoluble Constituent or Residue.
Ash, Water insoluble ash
Arsenic or lead
Loss on drying
Loss on ignition.
Effect of Impurities
Introduction of Inorganic Chemistry, History of Pharmacopoeia.pptxMs. Pooja Bhandare
Introduction of Inorganic Chemistry, History of Pharmacopoeia, Pharmaceutical Chemistry, Inorganic Chemistry:
IMPORTANTS OF INORGANIC CHEMISTRY, Introduction of Pharmacopoeia, Types of Pharmacopoeia, History of pharmacopoeia, HISTROY OF INDIAN PHARMACOPOEIA
Content of pharmacopoeia Introduction including general Notices
Monographs of the official drugs
Appendices
Polyploidy, mutation and hybridization with reference to medicinal plants. PH...Ms. Pooja Bhandare
Polyploidy, mutation and hybridization with reference to medicinal plants. PHARMACOGNOSY & Phytochemistry-I (BP405T)Unit-IIPart-4
Polyploidy reference to medicinal plants.
Types Of Polyploidy
A. Euploidy
a.Autopolyploidy
b. Allopolyploidy
B. Aneuploidy
1. Causes Of Polyploidy
2. Non-disjunction in mitosis
3. Non-reduction in meiosis
4. Polyspermy
5. Endo-replication or Endo- reduplication.
Factors Promoting Polyploidy
1. Physical factor
2. Chemical factor
3. Biological factor
Physical factor:-
Temperature :- heat temperature & cold temperature
Centrifugation
X-rays
Gamma rays
Cosmic rays
Ionizing & non-ionizing radiations
UV-radiations
Chemical factor:-
Alkylating agents:- nitrogen & sulphur mustard
Acridines
Proflavins
Nitrous acid
Colchicines[6]
Colchicines (Poisonous alkaloids):-
Biological factor
Mode of reproduction
Mode of fertilization
Breeding system present (Hybridization)
Growth habit of the plant
Size of chromosomes
Application Of Polyploidy
Mutation breeding
Seedless fruits production
Bridge crossing
Ornamental & forage breeding
Disease resistance through aneuploidy
Industrial application of polyploidy
mutation reference to medicinal plants
Type of mutations:
1. Spontaneous and induced mutations.
2. Recessive and dominant mutations.
3. Somatic and germinal mutations.
4. Forward, back and suppressor mutation.
5. Chromosomal, genomic and point mutations
Application Of Mutation:
Hybridization reference to medicinal plants
The following steps are involved in hybridization of plant:
Choice Of Parents:.
Selfing Of Parents
Emasculation:.
Bagging:
Crossing Or Cross Pollination
Labelling
Collection Of Hybrid Seeds
Significance of Hybridization
PHARMACOGNOSY & Phytochemistry-I (BP405T)Unit-IIPart-2.FACTORS AFFECTING CULTIVATION
1. Altitude
2.Temperature
3. Rainfall
4. Day Length and Day Light
5. Soil
6. Soil Fertility
7. Fertilizers and Manures
a) Chemical fertilizers
(b) Manures
(c) Biofertilizers
8. Pests and Pests Control
a. Microbes
b) Insects
C) Non insect pests
d) Weeds
9. Other Factors that Affect the Cultivated Plants
a. Air Pollution
b. Herbicide
Cultivation and collections of drugs of natural origin..pptxMs. Pooja Bhandare
PHARMACOGNOSY & Phytochemistry-I (BP405T)Unit-IIPart-1Cultivation and collections of drugs of natural origin.
Advantages of cultivation
Methods of Plant Propagation
1.Sexual method (seed propagation)
2. Asexual method
Methods of sowing the seeds
Broadcasting Dibbling Miscellaneous
Special treatment to seeds
Asexual method.
Asexual method of vegetative propagation consists of three types:
a) Natural methods of vegetative propagation.
b) Artificial methods of vegetative propagation.
c) Aseptic method of micropropagation (tissue-culture).
COLLECTION OF CRUDE DRUGS
HARVESTING OF CRUDE DRUGS
DRYING OF CRUDE DRUGS
(1) natural (sun drying) and (2) artificial
Artificial Drying
Drying by artificial means includes drying the drugs in
(a) an oven; i.e. tray-dryers;
(b) vacuum dryers and
(c) spray dryers.
GARBLING (DRESSING)
PACKING OF CRUDE DRUGS
STORAGE & PRESEVATION OF CRUDE DRUGS
Quality control of Drugs of Natural Origin. PHARMACognosy & Phytochemistry-I ...Ms. Pooja Bhandare
Quality control of Drugs of Natural Origin PHARMACognosy & Phytochemistry-I (BP405T)Unit-I Part-3.
CONTENTS
Adulteration
Evaluation of adulteration
Morphological / Organoleptic evaluation
Microscopic evaluation
Quantitative evaluation
Physical evaluation
Chemical evaluation
Biological evaluation
Adulteration is of two types:
Indirect or Unintentional adulteration
Direct or Intentional adulteration
Intentional adulteration may be due to the following reasons
adulteration using manufactured substances
substitution using inferior commercial varieties
substitution using exhausted drugs
substitution of superficially similar inferior natural substance
adulteration using the vegetative part of the same plant
addition of toxic materials
adulteration of powders
addition of synthetic principles
Evaluation of Crude Drugs
1. ORGANOLEPTIC EVALUATION
2. MICROSCOPICAL EVALUATION
Stomatal index Vein-islet number
Veinlet termination number
Palisade ratio
Quantitative Microscopy (Lycopodium Spore Method)
3.CHEMICAL EVALUATION
4. Physical Evaluation
I. Solubility
II. Optical Rotation
III. Refractive Index
III. Specific Gravity
IV Viscosity
V. Melting Point
VI. Moisture Content
VII. Ultraviolet Light
VIII. Ash Values
Total ash
Acid-insoluble ash
The water-soluble ash
IX. Extractive Values
X. Foreign Organic Matters
5. BIOLOGICAL EVALUATION
Toxicity
Oxytocic activity
Microbiological assays
Classification of Crude Drugs. HARMACognosy & Phytochemistry-I (BP405T)Unit-I...Ms. Pooja Bhandare
Classification of Crude Drugs.PHARMACognosy & Phytochemistry-I (BP405T)Unit-I Part-2.
A method of classification should be:
a) simple,
b) easy to use, and
c) free from confusion and ambiguities.
TYPES OF CLASSIFICATION.
1.Alphabetical classification
2.Taxonomical classification
3.Morphological classification
4.Pharmacological classification
5.Chemical classification
6.Chemotaxonomical classification
7. Serotaxanomical Classification
Animal Cell Culture: Growth of animal cells in culture. PHARMACEUTICAL MICROB...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-VPart-4
Animal Cell Culture: Growth of animal cells in culture.
Introduction: Histroy, The culture media used for animal cell culture are classified as,
Natural, Artificial, Synthesized
Natural Culture Media:
a. Blood Plasma:
b. Blood Serum:
c. Tissue Extracts:
Artificial Media
Some common examples of artificial media are,
Minimal Essential Medium (MEM),
CMRL 1066,
RPMI 1640.
Synthetic media re classified as,
Serum Containing Media.
Serum Free Media.
a. Serum Containing Media:
b. Serum Free Media:
Physicochemical Parameters needed for growth animal cell culture:
General procedure for cell Culture.
Isolation of the tissue:
Disaggregation of the Tissue:
Mechanical disaggregation
b. Enzymatic Disaggregation
. Trypsin based disaggregation or trypsinization:
Warm trypsinization:
Cold trypsinization:
Drawbacks of trypsin disaggregation:
B. Collagenase based disaggregation:
C. Chelating Agents:
3. Seeding of Culture:
Preservation of pharmaceutical products using antimicrobial agents. PHARMACEU...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-VPart-3
Preservation of pharmaceutical products using antimicrobial agents.
Introduction. Ideal Properties of Preservatives:
Antimicrobial Chemical Preservatives
Development of a Preservative System.
Factors affecting efficacy of a preservative: 1. Interaction With components of the formulation
2. Properties of the Preservatives:
3) Effect of Containers.
4) Type of microbes:
5) Influence of pH:
Challenge Test: Efficacy Test of Preservative : Medium used, Choice of test organism:
Preparation of the inoculum:
Procedure:
Interpretation of Results:
Assessment of microbial contamination and spoilage. PHARMACEUTICAL MICROBIOLO...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-VPart-2
Assessment of microbial contamination and spoilage.
Assessment of microbial contamination and spoilage
1. Physical and chemical changes:
2. Assessment of viable microorganisms in non-sterile products:
3. Sterility test:
4. Estimation of pyrogens:
Microbial Limit Tests:
Total Aerobic Microbial Count:
Membrane Filtration.
Plate Count Methods.
Pour Plate Method.
Surface spread Method.
Most Probable Number(MPN)
Types of spoilage, factors affecting the microbial spoilage of pharmaceutical...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-V Part-1
Types of spoilage, factors affecting the microbial spoilage of pharmaceutical products, source and type of contaminants. Introduction: Defintion Types of Microbial Spoilage:
1. Infection induced due to contaminated pharmaceutical products: Table no. 1.1 Common pathogens spoiling pharmaceutical products:
2. Physicochemical spoilage –
i) Viable growth ii) Gas production
iii) Colouration / Decolouration
iv) Odour formation
v) Taste change
3. Physical Spoilage:
Cracking of emulsion:
Odor changes
4. Biological spoilage:
Microbial Toxins
Microbial Metabolites
5. Chemical spoilage: Table 1.2 Susceptibility of pharmaceutical ingredients to microbial contamination
Factors affecting microbial spoilage
Size of contaminant inoculum
Nutritional factors
Moisture content
pH
Storage temperature
Redox potential
Packaging design
Sources and Types Of Contamination:
Personnel,
Poor facility design,
Incoming ventilation air,
Machinery and other equipment for production,
Raw material and semi-finished material,
Packaging material,
Utilities,
Different media used in the production process as well as for cleaning and Cleanroom clothing.
Microbiological Assay of Vitamin & Amino acid Assessment of a New Antibiotic...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T) Unit-IV Part-3
Microbiological Assay of Vitamin & Amino acid Assessment of a New Antibiotic: Introduction:
Principle
Microbiological Assay of Cynocobalamin (Vitamin B12):
Tritrimetric Method.
Turbidimetric Method.
Preparation of Standard Cynocobalmine stock solution:
Preparation of Basal Medium Stock Solution:
Test Solution of the material to be assayed Preparation of inoculum: Procedure of Titrimetric method: Turbidimetric Method: Microbiological assay of Amino acids. Assessment of a New Antibiotic.
Introduction:
MIC of an antibiotic is tested either by one of the following ways,
Liquid Dilution Method.
Solid Dilution Method
Principles and methods of different microbiological assay, methods for standa...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-IV Part-2 Principles and methods of different microbiological assay, methods for standardization of antibiotics.
Introduction: Principles Advantages of Microbial Assay: Disadvantages of Microbial Assay: MICROBIOLOGICAL ASSAY OF ANIBIOTICS PRINCIPLE Media used for antibiotics assay Standard Preparation. Buffer Solutions Preparation of the Sample Solution: Test Organisms Preparation of inoculum: Methods of preparation of test organism suspension: Assay Methods: Method A: Cup-plate or Cylinder Plate Method.
Method B: Turbidimetric or Tube assay Method
Designing of aseptic area, laminar flow equipment: Study of different source ...Ms. Pooja Bhandare
Designing of aseptic area, laminar flow equipment: Study of different source of contamination in aseptic area and methods of prevention, clean area classification. PHARMACEUTICALMICROBIOLOGY (BP303T)Unit-IVPart-1
Introduction: Designing of Aseptic Area . i) The clean-up area,
ii) The compounding area,
iii) The aseptic area,
iv) The quarantine area and
v) The packaging/labelling area.
Flow diagram of aseptic area. Floors, walls and ceilings, Doors, windows and services Personnel and protective clothing Cleaning and disinfection. Air Supply. Laminar flow equipment. Vertical laminar air flow bench
Horizontal laminar air flow bench
High Efficiency Particulate Air (HEPA) Filter. Operating Instructions Uses of Laminar Air Flow.Advantages of Laminar Air Flow.Limitations of Laminar Air Flow. Air flow pattern Unidirectional airflow
Non-unidirectional airflow
Combined airflow
Different Sources of Contamination in an Aseptic Area
1) Personnel:
2) Buildings and Facilities
3) Equipment and Utensils:
4) Raw Materials
5) Manufacturing Process:
Methods of Prevention of Contamination Clean Area Classification
Sterility testing products (solids, liquids, ophthalmic and other sterile pro...Ms. Pooja Bhandare
PHARMACEUTICAL MICROBIOLOGY (BP303T)Unit-IIIPart-6 Sterility testing products (solids, liquids, ophthalmic and other sterile products) according to IP, BP, USP.
Introduction: Test for Sterility. Culture Media. Fluid Thioglycollate Medium (FTM).
Alternative Thioglycollate Medium (ATM).
Soybean Casein Digest Medium (SCDM).
Tests for Culture Media:
Sterility of Media.
Growth Promotion Test.
Test for Bacteriostatic and Fungistatic.
Sterility Test Methods. Methods A: Membrane Filtration.
Method B: Direct Inoculation Pyrogen Test Methods. Rabbit Test. LAL Test.
Ethnobotany and Ethnopharmacology:
Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
New development in herbals,
Bio-prospecting tools for drug discovery,
Role of Ethnopharmacology in drug evaluation,
Reverse Pharmacology.
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The Roman Empire, a vast and enduring power, stands as one of history's most remarkable civilizations, leaving an indelible imprint on the world. It emerged from the Roman Republic, transitioning into an imperial powerhouse under the leadership of Augustus Caesar in 27 BCE. This transformation marked the beginning of an era defined by unprecedented territorial expansion, architectural marvels, and profound cultural influence.
The empire's roots lie in the city of Rome, founded, according to legend, by Romulus in 753 BCE. Over centuries, Rome evolved from a small settlement to a formidable republic, characterized by a complex political system with elected officials and checks on power. However, internal strife, class conflicts, and military ambitions paved the way for the end of the Republic. Julius Caesar’s dictatorship and subsequent assassination in 44 BCE created a power vacuum, leading to a civil war. Octavian, later Augustus, emerged victorious, heralding the Roman Empire’s birth.
Under Augustus, the empire experienced the Pax Romana, a 200-year period of relative peace and stability. Augustus reformed the military, established efficient administrative systems, and initiated grand construction projects. The empire's borders expanded, encompassing territories from Britain to Egypt and from Spain to the Euphrates. Roman legions, renowned for their discipline and engineering prowess, secured and maintained these vast territories, building roads, fortifications, and cities that facilitated control and integration.
The Roman Empire’s society was hierarchical, with a rigid class system. At the top were the patricians, wealthy elites who held significant political power. Below them were the plebeians, free citizens with limited political influence, and the vast numbers of slaves who formed the backbone of the economy. The family unit was central, governed by the paterfamilias, the male head who held absolute authority.
Culturally, the Romans were eclectic, absorbing and adapting elements from the civilizations they encountered, particularly the Greeks. Roman art, literature, and philosophy reflected this synthesis, creating a rich cultural tapestry. Latin, the Roman language, became the lingua franca of the Western world, influencing numerous modern languages.
Roman architecture and engineering achievements were monumental. They perfected the arch, vault, and dome, constructing enduring structures like the Colosseum, Pantheon, and aqueducts. These engineering marvels not only showcased Roman ingenuity but also served practical purposes, from public entertainment to water supply.
2. Content:
• Radiopharmaceuticals
Radio activity
Measurement of radioactivity,
Properties of α, β, γ radiations,
Half life, radio isotopes and study of radio isotopes - Sodium iodide I131 ,
Storage conditions, precautions & pharmaceutical application of radioactive
substances.
3. Radiopharmaceuticals.
• Radiopharmaceuticals, as the name suggests, are pharmaceutical formulations
consisting of radioactive substances (radioisotopes and molecules labelled with
radioisotopes), which are intended for use either in diagnosis or therapy or
diagnosis.
• The use of radioactive material necessitates careful and safe handling of these
products by trained and authorized personnel, in approved/authorized laboratory
facility as per the guide lines of Atomic Energy Regulatory Board (AERB) of
India.
4. • Radiopharmaceuticals are essential components of nuclear medicine
practice, where radiopharmaceuticals are administered to patients for
diagnosing, managing and treating number of diseases.
• Nearly 95% of radiopharmaceuticals are used for diagnostic purposes,
while the rest is used for therapy.
5. • Definitions and Terminology
• A nuclide (or nucleide, from nucleus, also known as nuclear species) is an
atomic species characterized by the specific constitution of its nucleus, i.e., by
its number of protons, Z, its number of neutrons, N, and its nuclear energy state.
• A radionuclide (radioactive nuclide, radioisotope or radioactive isotope) is an
atom that has excess nuclear energy, making it unstable.
• This excess energy can be used in one of three ways: emitted from the nucleus
as gamma radiation; transferred to one of its electrons to release it as a
conversion electron; or used to create and emit a new particle (alpha particle or
beta particle) from the nucleus
6. Isotopes
• Isotopes are variants of a particular chemical element which differ in neutron
number, and consequently in nucleon number.
• All isotopes of a given element have the same number of protons but different
numbers of neutrons in each atom.
• Isotopes of an element are atoms of same element with the same atomic
number ‘Z’ but different mass numbers ‘A’.
• They occupy the same place in the periodic table and have similar chemical
properties.
7. • Radioactive decay (also known as nuclear decay, radioactivity,
radioactive disintegration or nuclear disintegration) is the process by
which an unstable atomic nucleus loses energy by radiation.
• A material containing unstable nuclei is considered radioactive. Three of
the most common types of decay are alpha decay, beta decay, and
gamma decay,
• all of which involve emitting one or more particles.
8. Types of decay (Alpha, Beta and Gamma Radiations)
Radioactive rays were observed to be of three types: 1
1. Alpha rays, which could barely penetrate a piece of paper
2. Beta rays, which could penetrate 3 mm of aluminium
3. Gamma rays, which could penetrate several centimetres of lead
We now know that alpha rays are helium nuclei, beta rays are electrons, and
gamma rays are electromagnetic radiation.
9. Units of Radioactivity:
• The old unit of radioactivity was Curie (Ci), named after the scientists
Madame Marie Curie and Pierre Curie, the pioneers who studied the
phenomenon of radioactivity.
• One Ci is the number of disintegrations emanating from 1 g of Radium-226,
and is equal to 3.7 x 1010 Bq.
• In the International System (SI), the unit of radioactivity is one nuclear
transmutation per second and is expressed in Becquerel (Bq), named after the
scientist Henri Bequerel.
10. Measurement of Radioactivity
• The measurement of nuclear radiation and detection is an important aspect
in the identification of type of radiations (, , ) and to assay the
radionuclide emitting the radiation, suitable detectors are required. The
radiations are identified on the basis of their properties.
• e.g. Ionization effect is measured in Ionization Chamber, Proportional
Counter and Geiger Muller Counter.
• The scintillation effect of radiation is measured using scintillation
detector and the photographic effect is measured by Autoradiography.
11. Gas Filled Detectors:
1. Ionization Chamber:
2. Proportional Counters:
3. Geiger-Muller Counter
Ionization Chamber:
It is the simplest gas filled detector which is based on the collection of all
the charges created by direct ionization of the gas molecules through the
application of electric field.
12. • It consists of chamber filled with gas like Argon, Helium or Air etc.
Ionization chamber is fitted with two electrodes kept at different electric
potential (50-100V for each cm of distance between two electrodes) and a
measuring device to indicate the flow of current. Radiations bring about
ionization of gas molecules or ions which cause emission of electrons
which in turn reveals the changes in electric current.
13. • Advantages:
1. Good Uniform response to a radiation over a wide range of energy.
• Disadvantages
1. Relatively weak output pulse
14. 2. Proportional Counters:
• It is the modified form of ionization chamber.
• Operate at high voltage (1000-2000v).
• It is device used to detect charged particle having low ionization power (i.e.,
).
• Filling gas 90% Ar and 10% methane
• Principal : When voltage between cathode anode is sufficiently increases,
primary ion will produce by interaction of gas particles . They gain sufficient
energy to further collide with gas molecule and produce secondary ions and
give rice to detector pulse.
• Advantage: Detect low energy particle.
• High ionising power
• Disadvantages: Require high degree of stable voltage because slight change in
voltage change the gas multiplication.
15. 3. Geiger-Muller Counter:
• GM counter was developed by Geiger and Muller in Germany in the year 1928.
• It is a devise used to detect and measuring ionizing radiation.
• It is used to all type radiations α, β, γ easily.
• It is the oldest radiation detector due to its low cost, simplicity and in case of operation; it is the best detector among all.
Principle:
• A GM counter consists of a GM tube, sensing element which detects the radiation and processing electronics which displays
the result. The GM tube is filled with an inert gas such as Helium, Neon or Argon at low pressure, to which a high voltage
(450-500 V) is applied.
• The tube conducts electrical charge when a particle or photon of incident radiation makes the gas conductive by ionization.
The ionization considerably amplified within the tube to produce easily measured detection pulse, which is fed to processing
electronics and display the result.
16. Construction:
• It consists of a cylinder 1-2 cm in diameter of stainless steel or glass coated
with silver on inner side which acts as cathode.
• Internally a tungsten wire is suspended which is mounted at one end with a
glass bead, act as anode.
• Cylinder is filled mixture of gas (argon and helium generally used) at low
pressure which also contain a small amount of quenching vapours.
17.
18. Working:
• Radiations when enter the tube through a thin section also called as window causes
the ionization of gas molecules. From these ionized atoms or molecules, an electron
is knocked out of the atom and the remaining atom is positively charged.
• When the high voltage is applied across the electrode (300-1300), the electrons and
positively charged ions are attracted towards anode and cathode respectively.
• Hence, each particle of radiation produces a brief flow or pulse of current which can
be transmitted to radioactive sensor via an interface, which is finally recorded in
computer.
• All pulses from a GM counter are of same amplitude for any incident radiations.
Disadvantages:
• A GM counter cannot distinguish between types of different radiation and their
energy. However, the multiplication factor is a big advantage in simple radioactive
counting.
19. Types of GM Counter
I. End window type: For alpha particle, low energy
beta particle and low energy x-ray.
They have window at one end covered with thin
material through which low penetrate rays can easily
pass.
II. Window less type: These type of tube would not
have any windows and thickness would be in the range
of 1-2mm.
• This type of tube used in the detection of high
penetrating radiation.
20. • Quenching vapours are used:
(a) To prevent the false pulse that may be produced due to positive ion reaching the cathode.
(b) To absorb photons emitted by exciting atoms and molecules returning to their ground state.
• Note: Both Chlorine and Bromine are commonly used as quenching agents.
Ethyl alcohol and Ethyl are commonly used as quenching agents.
• Depending on purpose, different counters are used, like:
1. For counting the radioactive solid source, the end window type GM counter has been used in which
window has been made up of Aluminium alloy (7 mg /cm2), Mica or may be thin glass bubble (15
mg/cm2).
2. For counting beta and gamma particles, thin glass walled counters may be used. These have been
normally of about 1 cm in diameter, having a glass wall of 20-40 mg/cm2 thickness and tube is coated on
inside with Graphite to form cathode.
3. In order to count radioactive liquids, the counter having the capacity of 10 cm3 is used. In such a
counter, 3% solution of Uranium salt gives nearly 10,000 counts per minute.
4. To count radioactive gases, radioactive gas is introduced together with counting gas. For more
efficient gamma counting, counter having lead or copper cathode have been used.
21.
22. Scintillation Detector:
• When high energy radiation or photons is incident on certain substance, a flash
of light is emitted by the phenomenon called fluorescence or phosphorescence.
• This output light can be used as a measure of adsorbed radiation on
scintillation detector. This emitted light when enters into photo-multiplier tube;
it multiplies and amplifies even a small signal. So it becomes possible to
measure alpha, beta or gamma radiation by scintillation detector.
23.
24. Important properties of good scintillation detector are:
• High scintillation efficiency.
• The light produced should be proportional to the light incident on detectors.
• Detector material should be transparent to the wavelength range and must not
produce any interference in the resultant spectra.
• Short decay time of the induced fluorescence can be increased by dynodes which
are made up of phosphor or fluor which multiplies the electrons when strike to
them. Hence various inorganic and organic scintillation detectors can be used to
measure the incident radiation.
• Inorganic scintillation detectors like alkyl halides are most common compounds.
e.g. Sodium iodide, Cesium iodide, Lithium iodide.
• Organic Scintillators like plastic scintillators have good scintillation property but
stilbene have low scintillation property.
25. Semiconductor Detector
• It is a diode of n (electron rich) and p (electron deficient) semiconductors. In a
semiconductor the band gap is very small of the order of 2-3 eV and therefore
large numbers of electron hole pairs are formed, thus, giving rise to very good
resolution to these detectors. Application of a reverse bias across the diode
causes transport of electrons towards the n-end and that of ‘holes’ towards p-
end.
• The absorption of incident radiations results in the formation of electron and
hole pairs which move under the influence of applied electric field. The
collection of electrons at the electrode produces a voltage pulse, which is
proportional to the intensity of the incident radiation.
26.
27. Solid State Detectors:
They have high resolution, compactness and easy interpretation of output signal.
(a) Cerenkor Detector: These are based upon light which is emitted by fast charged
particles through an optically transparent medium with refractive index of more than
one.
(b) Thermoluminescence dosimeters: These are made up of those inorganic crystals
in which electron hole pairs have been formed due to radiations which can trap these
pairs and on heating lead to emission of light. e.g. CaSO4:Mn, LiF, CaF2:Mn etc
(c) Track-etch Detector: Ionizing radiations having higher linear energy transfer
(LET), passing through a dielectric material create trail of damaged molecule along
their path. In some material, the tract can be visible upon etching in a strong acid or
alkali solution. The damaged molecular tracks are etched faster than the bulk and look
like a pits on the surface. These tracks can be counted by viewing through a
microscope. The commonly used track-etch materials are quartz, mica, silica glass,
flint glass, polyethylene terephthalate, lexan, markrofol, cellulose triacetate, cellulose
nitrate.
28. 4. Autoradiography
• It is a bioanalytical technique used to visualize the radiolabelled substance by
using suitable radioisotopes.
• Principal: Radioisotopes will be emit and emitted radiation will ionize the
photographic emulsion result is the formation dark spot.
• Example of photographic emulsion : Silver halide (Ag x)+ Gelatin
• Agx Ag + x ------------------ Ag
Dark Spot
-
+
radiation
29. • Method.
1. Cover the radioactive sample with photographic emulsion.
2. Radioactive part of sample activate the Agx particle nearby
3. The result is the product of Ag ion into Ag atom leaving dark colour band.
4. The slide us washed with fixer to get insoluble silver atom and observe under
autoradiogram.
+
30.
31. • Certain precautions must be taken:
(i) Radioactive material should never be touched with hands but handled by
means of forceps.
(ii) Food contaminated with radioactive material can cause serious damage to
internal organs, so avoid any food intake, drinking and smoking within the lab.
(iii) Sufficient protective clothing or shielding must be used while handling the
material.
(iv) Radioactive material should be kept in labeled containers and must be
shielded.
(v) Area of storage must be under proper supervision.
(vi) Disposal of radioactive material is done with great care.
32. Properties of α, β, γ radiations
• Properties of α, β, γ radiations: - All substances are made of atoms. These have electrons (e)
around the outside, and a nucleus in the middle. The nucleus consists of protons (p) and
neutrons (n), and is extremely small. (Atoms are almost entirely made of empty space!). –
• In some types of atom, the nucleus is unstable, and will decay into a more stable atom. This
radioactive decay is completely spontaneous. - When an unstable nucleus decays, there are
three ways that it can do so.
• It may give out:-
1. an alpha particle (α)
2. a beta particle (β)
3. a gamma ray (γ)
33. Alpha particles (α)
• Alpha particle radiation consists of two neutrons and two protons, as they are
charged they are affected by both electric and magnetic fields.
• The speed of the α particle depends very much on the source, but typically are
about 10% of the speed of light.
• The capacity of the α particle to penetrate materials is not very great, it usually
penetrates no more than a few centi metres in air and is absorbed by a
relatively small thickness of paper or human skin. However, because of their
speed and size, they are capable of ionising a large number of atoms over a
very short range of penetration.
• This makes them relatively harmless for most sources that are about a metre or
more away, as the radiation is easily absorbed by the air.
• But if the radiation sources are close to sensitive organs α particle radiation is
extremely dangerous.
34. Beta-particles (β)
• Beta-particle radiation consists of fast moving electrons. Every β -particle
carries either one negative or one positive electronic charge (β 1.6 × 10-19
coulomb: -e, +e). They are affected by electric and magnetic fields.
• The speed depends on the source, but it can be up to 90% of the speed of light.
• β particles can penetrate up to 1 m of air. They are stopped by a few millimetres
of aluminium or perspex.
• Their ionising capacity is much less than that of β radiation. They are very
dangerous if ingested.
35. Gamma radiation (γ)
• Gamma radiation does not consist of charged particles, it is a form of very short
wavelength electromagnetic energy. They travel at the speed of light (3 × 108
m/s).
• Gamma radiation is very difficult to stop, it takes up to 30mm of lead. Although
the ionising capacity of γ radiation is considerably smaller than that of beta-
radiation, their high penetration power means that they are dangerous even at a
distance.
• They can penetrate our bodies and hit sensitive organs. They are particularly
dangerous if ingested or inhaled.
36. Half –life of Radioelement
• The decay of individual atoms of radioactive substance has been found to be
irregular. If a certain amount of radionuclide is taken and the number of
disintegration per second is measured, it is found that, after certain time, half of
the original atoms would have got disintegrate and only half of the original
active atom would be left behind.
• The number of disintegrations per second will also now be half of the original
value.
37. • The decay time of radionuclide to its half has been constant irrespective of the
quantity present. The time is termed as half-life of the radionuclide.
𝑡1/2 =
0.693
γ
Where γ is disintegration constant in unit of 𝑠𝑒𝑐−1
• Half-lives for various radionuclides vary considerably; Polnium-212 half-life
of 3x 10−7 seconds, iodine 131has 8 days, Zn 65-150 days, Na 22-2.6 years
while uranium 238 has 4.5 x 104 years.
38. SODIUM IODIDE (I131)
• Synonym: Radioactive iodine
Out of all radioactive isotopes of Iodine, I131 is most commonly used. It is used as an aqueous solution of sodium iodide
having sodium thiosulphate in addition as a reducing agent.
Standards: It should not contain less than 90% and not more than 110% of labelled amount of Iodine-131 as iodide which is
expressed in microcuries or millicuries at the time indicating in the labelling.
• Method of Preparation:
• The first production of Iodine-131 took place in France in the year 1949 at the Fort de Chatillon, the site of the first Zoe
atomic reactor, before it was transferred to the nuclear research centre at Saclay. The isotope has been used since 1942,
however, in the treatment of thyroid cancer.
• Most I-131 is prepared in nuclear reactor by neutron-irradiation of a natural Tellurium target. Irradiation of natural
tellurium produces almost entirely I-131 as the only radionuclide with a half-life longer than hours. Ultimately in 8.02 days
it gets converted into Xenon-131 (stable isotope).
Te130 Te131 I131 Xe131
(n y) β β γ
39. • Properties:
1. It forms a colorless solution.
2. I131 have half-life of 8.4 days and emits beta and gamma radiations.
3. Its solution is having pH range of 7 to 10.
• Assay:
It is possible to determine its activity, using suitable counting equipment by comparison with a standardized I-131 solution or by
measurement of an instrument calibrated with the aid of such solutions. Iodine-131 has been emitting both beta and gamma particles in
its decay process. Radioactivity has to be recorded on a counting assembly which is having either a Geiger-Muller counter or a
scintillation detector used as a sensing unit and an electronic sealing device.
Hyperthyroidism Treatment by I131:
• Iodide inhibits the release of thyroid hormone and forms the basis for its use in hyperthyroidism. All the isotopes of iodine are
rapidly taken up by thyroid follicles. Radioactive iodine i.e. I131 is available as NaI131 solution and is administered orally.
• The absorption of I131 leads to highly localized destruction of thyroid follicles due to
β-particles emission. This property of I131 has promoted radioactive iodine as a therapeutic alternative in surgical removal of the
gland. The radio iodine therapy is considered advantageous over surgery because of the simplicity of its procedure, its applicability
to patients, avoidance of surgical risks and complications.
40. Sodium iodide-131 solution and capsule:
• Sodium iodide (I131) are suitable both for oral or i.v. administration. The solution is clear and colourless, but as the time
passes both the solution and glass may get darken due to the effect of radiation. The pH of solutions varies between 7.5-9.0.
• For injection, a suitable preservative such as benzyl alcohol is added. A reducing agent such as sodium thiosulphate is also
added to the solution, to prevent the oxidation of sodium iodide in aqueous solutions.
• Potassium salt, iodide and iodate have been acting as a carrier for iodide ions and for iodate ions present in the sodium
iodide I131 solution.
• Sodium iodide (I131) capsules are prepared by evaporating an alcoholic solution of sodium radio-iodide directly on the
walls of the capsule or on inert capsule filling material.
• Radioactive Identification:
• The spectrum of I131 has been complex but the most abundant type of photon is having energy of 0.364 MeV. It is
possible to determine the energy in a spectrometer by detecting -radiation with a scintillation counter which is having a
thallium activated. The γ-ray scintillation spectrum of sodium iodide (I131) solution has been found to be identical to that of
specimen of I131of known purity, which exhibits major photoelectric peak, having energy of 0.365 MeV.
41. Handling and Storage of Radioactive Material:
• Great care must be taken in handling and storage of radioactive material so as
to protect the people from its harmful effects.
• The radioactive materials are stored in remote areas such that it should be away
from exposure to human beings.
• and -emitters are stored in thick glass such that shielding effect is provided,
while -emitters are stored in lead containers.
• The area of radioactive material should be tested for intensity of radioactivity.
• Exposure to radioactive radiation can cause blood cancer to persons.
• Lead shielding is required while handling with radioactive substances.
• Shielding effect can also be achieved by water layer and concrete blocks. Water
layer blocks only radiation which allows visible light to pass while concrete
blocks all the radiations.
42. Storage of Radioactive Substances –
• Radiopharmaceuticals should be kept in well-closed containers and stored in an
area assigned for the purpose.
• The storage conditions should be such that the maximum radiation dose rate to
which persons may be exposed is reduced to an acceptable level.
• Care should be taken to comply with national regulations for protection against
ionizing radiation.
• Radiopharmaceutical preparations that are intended for parenteral use should be
kept in a glass vial, ampoule or syringe that is sufficiently transparent to permit
the visual inspection of the contents. Glass containers may darken under the
effect of radiation.
43. Precautions For Handling Radioactive Substances
• The following guidelines provide information on the safe handling of radioactive
substances. They are based on the relevant legislation and on the Code of Practice
for Handling Radioactive Substances.
• The radioactive substances used should comply with the following characteristics:
Radiotoxicity must be as low as possible.
Short-living isotopes are preferred to long-living ones
The amounts used must be kept to a minimum.
• Never work alone in a radioactive lab, especially not outside normal working hours.
Always make sure to have someone nearby in case of emergency.
44. • Take all precautions to prevent radioactive contamination:
Always separate radioactive activities from non-radioactive activities.
As far as possible, limit the area where radioactive substances are used and mark the
area, e.g. by using containers with absorbent paper.
Apply a radiation symbol to any containers and items that have come into contact
with radioactive substances.
Never bring documents such as notes into the radioactive zone.
• When handling radioactive materials, always wear the appropriate protective
clothing:
Wear a lab coat. If there is a risk of serious contamination, wear disposable clothing.
Store your lab coat away from your regular clothes.
Always wear gloves when handling radioactive substances. Regularly check the
radiation level of these gloves. Never touch anything with potentially contaminated
gloves; use paper tissues instead.
Wear shoe covers in rooms where the floor may be contaminated.
Keep personal items such as handbags, etc., outside the lab.
45. • Use appropriate radiation shields. Return the stock solution to storage
immediately after removing the amount needed.
• To avoid internal contamination, strict hygiene is essential when handling
radioactive materials
Eating, smoking, drinking, and applying cosmetics are prohibited in radioactive
labs.
Never pipette by mouth. Use pipetting devices instead.
Wash your hands thoroughly when you leave the lab.
• Regularly check the radiation level of your working area and all objects used,
or at least at the end of each working day. Replace contaminated absorption
paper. Decontaminate contaminated objects.
• Dispose of all radioactive waste in the appropriate containers. Limit the amount
of waste to a bare minimum. Separate short-living and long-living radioactive
waste.
46. Labelling of Radioactive Substances
• Every radiopharmaceutical preparation must comply with the labelling requirements
established under Good Manufacturing Practice.
• The label on the primary container should include:
1. A statement that the product is radioactive or the international symbol for
radioactivity
2. The name of the radiopharmaceutical preparation;
3. Where appropriate, that the preparation is for diagnostic or for therapeutic use;
4. The route of administration;
5. The total radioactivity present at a stated date and, where necessary, time; for
solutions, a statement of the radioactivity in a suitable volume (for example, in
MBq per ml of the solution) may be given instead;
6. The expiry date and, where necessary, time;
7. The batch (lot) number assigned by the manufacturer;
8. For solutions, the total volume.
47. • The label on the outer package should include:
1. A statement that the product is radioactive or the international symbol for
radioactivity o The name of the radiopharmaceutical preparation;
2. Where appropriate, that the preparation is for diagnostic or for therapeutic use;
3. The route of administration;
4. The total radioactivity present at a stated date and, where necessary, time; for
solutions, a statement of the radioactivity in a suitable volume (for example, in
MBq per ml of the solution) may be given instead;
5. The expiry date and, where necessary, time;
6. The batch (lot) number assigned by the manufacturer;
7. For solutions, the total volume;
8. Any special storage requirements with respect to temperature and light;
9. Where applicable, the name and concentration of any added microbial
preservatives or, where necessary, that no antimicrobial preservative has been
added.
48. Pharmaceutical Application Of Radioactive
Substances
Treatment of Cancers and Tumours
• Americium 241 used as antineoplastic.
• Californium 252 used as antineoplastic.“
• Cobalt 60 used as antineoplastic.
• Gold 94 used as antineoplasatic.
• Holmium 66 (26 h) being developed for diagnosis and treatment of liver tumours.
• Iodine-125 (60 d) used in cancer brachytherapy (prostate and brain).
49. Treatment of Thyroid Disease with Iodine 131
• Iodine-131 is therapeutically used for to treat thyroid cancer, hyperthyroidism
(including Graves’ disease, toxic multinodular goiter, and toxic autonomously
functioning thyroid nodules), and Nontoxic multinodular goiter.
Palliative Treatment of Bone Metastasis
• Various radioisotopes and pharmaceuticals are used to deliver palliative treatment of
bone metastases, including samarium-153 (Sm-153), strontium-89 (Sr-89) chloride,
and phosphorus-32 (P-32) sodium phosphate. The two most common side effects
occurring from radiopharmaceutical therapy for metastatic bone disease are initial
increased bone pain (flare) and a decrease in WBC and platelet counts.
50. Treatment of Arthritis
• Erbium-169: Use for relieving arthritis pain in synovial joints - Diagnostic
Radiopharmaceuticals
• Ammonia N 13 Injection used for diagnostic coronary artery disease.
• Chromium 51 used for diagnosis of pernicious anaemia.
• Holmium 166 used for diagnosis and treatment of liver tumours.
• Iodine 125 used diagnostically to evaluate the filtration rate of kidneys.