Water is synonymous with ‘life’ as no life can exist on earth without air and water. Though water is the most abundant natural resource, the quantity of water that is apt for consumption is becoming scarce because of an upsurge in population level. Thus, the quality of drinking water clarifies, whether it is suitable for being consumed or not. Therefore, it needs to be tested before consumed. Sigmatest, the best water testing lab, carries drinking water tests in India at a very affordable price and effectively.
Page | 30
TESTS CONDUCTED IN MICROBIOLOGY LABORATORY OF ACI
❖ Bacterial endotoxin test (BET/LAL test/ Pyrogen Test)
❖ Microbial limit test for non-sterile pharmaceutical products (syrup, suspension, cream,
ointment, gel, tablet and raw materials)
❖ Microbiological assay of antibiotics
❖ Sterility test of sterile pharmaceutical products
❖ Sampling of water (purified water, potable water and water for injection)
❖ Sampling of raw materials
❖ Total organic carbon analysis (water for injection, purified water)
❖ Chemical analysis of water
❖ Environmental monitoring, settle plate
❖ Personal hygiene monitoring
❖ Surface monitoring
❖ Liquid borne particle count for WFI
❖ Preservative efficacy test
Media Used:
NON SELECTIVE MEDIA SELECTIVE MEDIA
R2A Agar Xylose Lysine Deoxycholate
Sabouraud dextrose agar Brilliant green lactose bile broth
Tryptone Soy Agar Bismuth sulphite agar
Tryptone Soy Broth
Eosine methylene blue agar
Thioglychollate medium Cetrimide agar
MacConkey agar
Triple sugar iron agar
Mannitol salt agar
Enterobacteriaceae enrichment broth
Page | 31
Figure 11: Selective & Non selective media used in ACI
BACTERIAL ENDOTOXIN TEST
PRINCIPLE
BET test is used to detect or quantify bacterial endotoxins that may be present in the sample
to which the test is applied. Endotoxin is a toxic substance found in the outer cell membrane
of Gram negative bacteria (Lipopolysaccharide, LPS) when they disintegrated. The gel clot
method is a qualitative or semi-quantitative method, which detects the endotoxin based on
clotting of the Limulus Amoebocyte Lysate (LAL) reagent in presence of endotoxin when
incubated. LAL reagent is prepared from lysate of the circulating amoebocytes of the
horseshoe crab Limulus polyphemus. When exposed to minute quantities of endotoxin, the
lysate increases in opacity, viscosity and forms gel depending on the concentration of
endotoxin. The concentration of endotoxin required to cause the lysate to clot under standard
conditions is the labeled sensitivity of LAL reagent.
hydrocolloid impression materials, agar and alginate impression materials and properties of the same.
watch more
https://youtu.be/aaJ6gpQohcs
https://youtu.be/REMKSUty0cE
https://youtu.be/fv3_tWZPJIU
https://youtu.be/GeZIbCwqKYU
if you want me to make any ppt on any more topic do let me know on my youtube channel's comment section
Page | 30
TESTS CONDUCTED IN MICROBIOLOGY LABORATORY OF ACI
❖ Bacterial endotoxin test (BET/LAL test/ Pyrogen Test)
❖ Microbial limit test for non-sterile pharmaceutical products (syrup, suspension, cream,
ointment, gel, tablet and raw materials)
❖ Microbiological assay of antibiotics
❖ Sterility test of sterile pharmaceutical products
❖ Sampling of water (purified water, potable water and water for injection)
❖ Sampling of raw materials
❖ Total organic carbon analysis (water for injection, purified water)
❖ Chemical analysis of water
❖ Environmental monitoring, settle plate
❖ Personal hygiene monitoring
❖ Surface monitoring
❖ Liquid borne particle count for WFI
❖ Preservative efficacy test
Media Used:
NON SELECTIVE MEDIA SELECTIVE MEDIA
R2A Agar Xylose Lysine Deoxycholate
Sabouraud dextrose agar Brilliant green lactose bile broth
Tryptone Soy Agar Bismuth sulphite agar
Tryptone Soy Broth
Eosine methylene blue agar
Thioglychollate medium Cetrimide agar
MacConkey agar
Triple sugar iron agar
Mannitol salt agar
Enterobacteriaceae enrichment broth
Page | 31
Figure 11: Selective & Non selective media used in ACI
BACTERIAL ENDOTOXIN TEST
PRINCIPLE
BET test is used to detect or quantify bacterial endotoxins that may be present in the sample
to which the test is applied. Endotoxin is a toxic substance found in the outer cell membrane
of Gram negative bacteria (Lipopolysaccharide, LPS) when they disintegrated. The gel clot
method is a qualitative or semi-quantitative method, which detects the endotoxin based on
clotting of the Limulus Amoebocyte Lysate (LAL) reagent in presence of endotoxin when
incubated. LAL reagent is prepared from lysate of the circulating amoebocytes of the
horseshoe crab Limulus polyphemus. When exposed to minute quantities of endotoxin, the
lysate increases in opacity, viscosity and forms gel depending on the concentration of
endotoxin. The concentration of endotoxin required to cause the lysate to clot under standard
conditions is the labeled sensitivity of LAL reagent.
hydrocolloid impression materials, agar and alginate impression materials and properties of the same.
watch more
https://youtu.be/aaJ6gpQohcs
https://youtu.be/REMKSUty0cE
https://youtu.be/fv3_tWZPJIU
https://youtu.be/GeZIbCwqKYU
if you want me to make any ppt on any more topic do let me know on my youtube channel's comment section
After the manufacturing of the drug, it is essential that these should be stored properly. The stability of drug during it’s storage depend on so many factor and proper packaging is one of them. The pharmaceutical products are in direct contact with the container and closures. So improper packaging and poor quality of container may lead to deterioration of the product.
Impression materials /certified fixed orthodontic courses by Indian dental ac...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
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After the manufacturing of the drug, it is essential that these should be stored properly. The stability of drug during it’s storage depend on so many factor and proper packaging is one of them. The pharmaceutical products are in direct contact with the container and closures. So improper packaging and poor quality of container may lead to deterioration of the product.
Impression materials /certified fixed orthodontic courses by Indian dental ac...Indian dental academy
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
www.indiandentalacademy.com
MANUFACTURING OF PARENTRALS
1. Formulation and Raw Materials:
Concept: The process begins with the formulation of the parenteral drug, determining its composition and concentration.
Raw Materials: High-quality pharmaceutical-grade raw materials, including active pharmaceutical ingredients (APIs), excipients, and solvents, are selected based on their compatibility and purity.
2. Sterilization of Raw Materials:
Concept: Due to the sterile nature of parenteral products, all raw materials, including the API and excipients, must undergo rigorous sterilization.
Methods: Common sterilization methods include autoclaving, filtration, and aseptic processing to ensure aseptic conditions throughout the manufacturing process.
3. Manufacturing Process:
Preparation: The formulation is prepared, and various components are weighed and measured precisely.
Mixing: The ingredients are mixed under controlled conditions to achieve a homogeneous blend, ensuring uniform distribution of the API and other components.
Filtration: The solution is then filtered to remove any particulate matter and ensure clarity.
Filling: The sterile drug solution is filled into vials, ampoules, or other suitable containers in a controlled environment, maintaining sterility.
4. Sterilization of Final Product:
Terminal Sterilization: The final product, in its container, undergoes terminal sterilization methods like autoclaving or gamma irradiation to eliminate any microbial contamination that may have occurred during the manufacturing process.
Ipqc tests for sterile formulations are as follows :
Leakage Test
Clarity Test
pH
Particulate Matter Injection
SterilityTest
Pyrogen Test
Content Uniformity & Weight
Volume Filled
The tests For Sterile products are as per IP, BP & USP
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NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
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3. PART.1
What is exactly micro-organisms attack paint, Paints have two major motivations: domestic and commercial.
Paint is used to protect the surface from corrosion, degradation, and discoloration in the areas where it has
been added.
The painted layers are disrupted or discolored as a result of weathering and deterioration, promoting the
development and work of biological organisms.
Throughout the degradation process, a variety of microbes such as microscopic bacteria, fungal growth,
algal growth, and protozoans are actively involved.
Temperature is a significant environmental factor that contributes to painting deterioration.
Micro-organisms attack paint and their behaviors can destroy water-based paints, reducing the paint’s
shelf life and the house’s longevity
Because of the use of different polymer compounds used in paint production, it is vulnerable to
corrosion and poses a risk to the environment.
4. Different Paint-Tests
Determination of the Microbial Condition of Paint, Paint Raw Materials, and Plant Areas Test (ASTM D 5588)
This test method covers a procedure for (micro-organisms attack paint)the determination of the microbial
condition (contamination or sterility) of raw materials used in the manufacture of paint, and the microbial
condition of paint and paint manufacturing areas.
This test method details protocols for obtaining samples for sterility testing from wet or dry products and
plant locations, conducting sterility testing on such samples to see whether they are polluted, evaluating
the degree of contamination, if any, and including a checklist for any measure of the form of
contamination present (bacterial, fungal, yeast, etc.).
This test procedure does not take any of the steps necessary to ensure the degree of sterility needed for
the most reliable results. It is recommended that you have some experience with microbiological
techniques.
5. Why this Test?
The use of polluted raw materials, water (especially recycled wash water), vessels, pipes, and equipment in the
manufacturing plant is often linked to paint spoilage in the container.
A simple method to determine the presence or absence of microorganisms in paint and coatings
manufacturing plants is needed.
This information allows the producer to pinpoint the source of pollution (raw materials or problematic
housekeeping areas in the plant) and work toward resolving the spoilage issue.
This test method details protocols for obtaining samples for sterility testing from wet or dry products and
plant locations, conducting sterility testing on such samples to see whether they are polluted, evaluating the
degree of contamination, if any, and including a checklist for any measure of the form of contamination
present (bacterial, fungal, yeast, etc.)
However, this test procedure does not take any of the steps necessary to ensure the degree of sterility
needed for the most reliable results.
6. TestingGuidelines
When collecting samples, take all appropriate precautions to prevent microbial contamination.
Wearing a face mask and sterilized gloves is an option. (Warning: Do not touch the swab near the cotton tip or
any other areas of the swab that can come into contact with the test sample.)
Microorganisms from the skin, clothes, and even the environment will contaminate the sample if exposed for
too long.
Do not strike every portion of the swab except the cap if the swab has one. Additional tests should be used
to confirm suspect results.
For each sample, use a fresh clean swab, tongue depressor, or spatula. Any sampling instruments cannot be
reused.
If you’re using gloves, make sure to throw them away after each use.
7. To prevent misleading contamination effects, limit the time clean products are exposed to the environment
while taking samples
Alternatively, the liquid sample could be transported to the sterile storage area in a sterilized bottle.
During sampling, handling, and transportation to the testing area, make sure no non-sterile items come into
contact with the liquid sample (for example, use a sterile pipet, etc. for material transfer to container, et
cetera).
Dry materials can be sampled in the same way as mentioned earlier. Wipe a wide section of the exterior of
the container clean with a clean rag or paper towel to sample unopened, dried raw materials in bags.
Inside the cleaned field, cut open the bag with a clean knife.
Scoop 10 to 15 g into a sterile plastic bag, close, and seal bag for transport to sterile testing area, using a
sterile tongue depressor or sterile spatula.
8. NOTE – To reduce the risk of inadvertent exposure, thoroughly clean the region of the bag to be sliced, as
well as the knife used to cut it, with isopropyl alcohol.
There is no requirement to sterilize machine surfaces when checking open containers of raw materials, vats,
barrels, and so on.
However, any bacteria found could have been added after the package was opened.
The presence of contaminants in samples obtained from machinery surfaces does not inherently imply that
the substance stored or processed within is also polluted.
9.
10. Result Evaluation
Bacterial contamination (aerobic) is generally characterized by milky spots of varying size (bacterial
colonies) on the agar surface. These are usually slimy or shiny in appearance.
Fungal contamination is generally characterized by spots that are usually filamentous and more fuzzy in
appearance, with the exception of yeasts which normally look similar to the bacterial colonies.
NOTE – If present, bacteria should grow on the TSA plates, but bacteria can also grow on the PDA or malt
extract plates, particularly if they are not acidified.
Fungi can also grow on the TSA plates, and yeast in particular can look like a bacterial contamination.
Differentiation between bacterial and fungal growth can require more sophisticated techniques than are
covered in this test method.
Assistance can be obtained from your biocide supplier.
11. StandardTest Method for Resistanceof EmulsionPaintsin the Containerto
Attack by Microorganisms– (ASTM D2574)
This test method covers the determination of the relative resistance of emulsion paints to attack in the
container by microorganisms.
Why Perform thistest?
Putrefaction, lowered pH, gas formation, and a drop in viscosity will all result from paint spotting in the
bottle.
This test method establishes a basic protocol for determining emulsion paints’ susceptibility to microbial
degradation.
12. The findings should allow:
(1) the paint manufacturer to choose an appropriate preservative; and
(2) the preservative provider to compare the efficiency of competitive and developmental preservatives in
emulsion paints.
This test procedure can be used for people who have a basic understanding of microbiology.
NOTE: The methods used have a significant impact on the reliability of the findings produced from this
research process.
Incorrect procedures may cause a sterile sample to appear polluted, or even worse, a contaminated
sample to appear sterile.
To check any doubtful findings, you can consult your biocide provider, raw material supplier, or an
independent testing laboratory.
The consistency of the formulation and raw materials will also influence the test results.