Dendrimers may be defined as synthetic three-dimensional hyper branched, globular macromolecule, which is characterized by its highly branched 3D structure that provides a high degree of surface functionality.
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Definition of polymer
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Polymeric micelle formation , mechanism , Case study , applications , Factors affecting formation of Polymeric Micelle , Method of preparation , Types of polymers used in Polymeric micelle
Definition of polymer
Types of Biodegradable polymers
Examples Biodegradable polymers
Application of Biodegradable polymers
Methods of Studying Polymer Degradation
Advantages of Biodegradable polymers
Dendrimers are nano-sized, radially symmetric molecules with well-defined, homogeneous, and monodisperse structure consisting of tree-like arms or branches.
The second group called synthesized macromolecules ‘arborols’ means, in Latin, ‘trees’. Dendrimers might also be called ‘cascade molecules’
Dendrimers are nearly monodisperse macromolecules that contain symmetric branching units built around a small molecule or a linear polymer core
‘Dendrimer’ is only an architectural motif and not a compound. Dendrimers have gained a broad range of applications in supra molecular chemistry, particularly in host-guest reactions and self-assembly processes.
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Dendrimers are considered as the Polymers of 21st century, which ease the process of drug discovery, as we know that current drug discovery techniques takes years of time in inventing new drugs, this new Dendrimers technique help drug discovery companies and pharmaceutical industries to speed up their drug discovery process and provide better results
COMPLETE DESCRIPTION ABOUT DENDRIMERS ALONG THEIR ROLE IN CURRENT MEDICAL SYSTEM,THEIR USEAGE IN CHEMOTHERAPUTIC PURPOSES ETC IS PROVIDED IN THIS PRESENTATION.
MD. ABU JAR GIFARI
Ph.D. Student
Dept. of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences
Prince of Songkla University
Hat-Yai, Songkhla, Thailand 90110
Phone: +660969247553
Email: agifari50@gmail.com
Dendrimers is an advanced source of pharmaceutical dosage forms. It improves the ease of drug delivery and better patient compliance. This technique can be used as the prodrug. It can be better used in Anti-Cancer therapy for better results.
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
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Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
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Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
2. CONTENT
INTRODUCTION
NEED OF DENDRIMERS
METHODS OF SYNTHESIS
MECHANISMS OF DRUG DELIVERY
GENERATION
TYPES OF DENDRIMERS
PROPERTIES OF DENDRIMERS
CHARACTERIZATION OF DENDRIMERS
APPLICATIONS
REFERENCES 2
3. The word “dendrimer” originated from two Greek words,
dendron :- meaning tree,
meros:- meaning part or segment.
Dendrimers are a new class of polymeric materials. They are
highly branched, monodisperse , artificial
macromolecules.
Dendrimers may be defined as synthetic three-dimensional
hyper branched, globular macromolecule, which is
characterized by its highly branched 3D structure that
provides a high degree of surface functionality.
3
4. HISTORY
In 1978, Vogtle and co-workers was first introduced
chemistry of Dendrimer .
In 1980, Donald Tomalia and co-workers discovered, these
hyper branched molecules were called dendrimers.
In 1985, Vogtle synthesized the first family of dendrimers
the first “cascade molecules”.
At the same time, Newkome’s groupindependently reported
synthesis of similar macromolecules.
They called them arborols from the Latin word ‘arbor’ also
meaning a tree.
The term cascade molecule is also used, but ‘dendrimer’ is
the well established one.
4
5. Dendrimers possess three distinguished components,
namely
(i) An initiator core.
(ii) Interior layers:- composed of repeating units, radically
attached to the interior core(generations).
(iii) Exterior layers :- attached to the outermost interior
generations (terminal functionality).
5
6. NEED OF DENDRIMERS:-
Nano-particle drug-delivery systems are most popular one.
However reticuloendothelial system (RES) uptake, drug
leakage, immunogenicity, haemolytic toxicity,
cytotoxicity, restrict the use of these nanostructures.
These are overcome by surface engineering the dendrimer
such as Polyester dendrimer, Glyco-dendrimers, PEGylated
dendrimers etc.
The bioactive agents can be easily encapsulated into the
interior of the dendrimers.
or
Chemically attached i.e. physically adsorbed on to the
dendrimer surface.
6
7. • Traditional method dendrimer synthesis are:
Michael reaction
Williamson ether synthesis.
Modern techniques are :
solid-phase synthesis,
organosilicon chemistry,
organo-phosphorus chemistry.
MANUFACTURE COUNTRY DENDRIMERS TRADE
MARK
NAME
CORE
MOLECULE
Dendritech TM U.S.A. PAMAM
dendrimers
Starburst
dendrimers
Ethylenediamine
(EDA) core
DSM Netherlands PPI
dendrimers
Astramol
TM
Butylenediamine
(BDA) core
7
8. METHODS OF SYNTHESIS:-
1) Divergent method.
2) Convergent method.
3) Hypercores & branched monomers method.
4) Double Exponential And Mixed Growth.
5) Other accelerated growth technique.
8
9. Core surface activation Dendrimer
molecule
Dendrimers starts from the central core and extends toward the surface
i.e. diverging into space.
Two step process:
Activation of functional surface groups
Addition of branching monomers units.
Divergent approach is successful for the production of large quantities
of dendrimers.
It causes some difficulties in the purification of the final
product.
1) Divergent method
9
10. Surface unit Monomers Core molecule Dendrimer
2) Convergent method
Dendrimer starting from the end groups and progressing inwards.
When the growing wedges are enough large, attached to a suitable core
to give a complete Dendrimer.
The convergent methodology also suffers from low yields in the
synthesis of large structures.
Advantages:
1.Relatively easy to purify the desired product.
10
11. 3) Hypercores & Branched Monomers Technique
Frechet group continued their efforts on research of
hypercore & branchad monomers.
This method involves the pre assembly of oligomeric species,
which can then be linked together to give dendrimer.
These monomers allow the to design synthetic strategies that
are more convergent in classical synthetic sense of world.
11
12. 4) ‘Double Exponential’ And ‘Mixed’ Growth
Double exponential growth, similar to a rapid growth
technique for linear polymers, involves an AB2 monomer
with orthogonal protecting groups for the A and B
functionalities.
This approach allows the preparation of monomers for
both convergent and divergent growth from a single
starting material.
These two products are reacted together to give an
orthogonally protected trimer, which may be used to repeat
the growth process again.
12
13. This is two step approach designed by frechet.
In this approach two different monomers are used so as to
avoid the need of an activation step between growth steps.
The two monomeric units are AB2 &CD2.where A&D
reacts to form bond under required conditions while B&C
are stable, where B&C reacts to form bond while A&D
remain stable.
In this technique the hindrance likely to be experienced is
that difficulty of finding a set of reactions,which conform
to above criteria.
5) Other Accelerated Growth Techniques
13
14. The first synthesized dendrimer was Polyamidoamines(PAMAMs)
They are also known as starbust dendrimers.
Ammonia is used as the core molecule & In the presence of methanol, it reacts
with methylacrylate and then ethylenediamine is added By repeating .
The Michael addition & amidation reaction step by step, high generation
dendrimers can be obtained .
Due to their multivalent and monodisperse character, dendrimers have wide
interest in the field of chemistry and biology, especially in applications like drug
delivery, gene therapy and chemotherapy.
14
15. Mechanisms of Drug Delivery
Simple encapsulation:-It directly encapsulates guest
molecules into macromolecule interior.
Electrostatic interaction:-Surface functional groups
enhances solubility of hydrophobic drugs by electrostatic
interaction e.g. Ibuprofen, ketoprofen, indomethacin.
Covalent conjugation:-The drug is covalently bound to
dendrimers & its cleavage occurs via chemical or
enzymatic cleavage of hydrolytically labile bonds. It allows
tissue targeting & controlled delivery as drug-dendrimer
conjugate diffuse slower than the free.
15
16. GENERATION:-
The number of focal points when going from the core towards the
dendrimer surface is the generation number.
That is a dendrimer having five focal points when going from the centre
to the periphery is denoted as the 5th generation dendrimer.
Here, we abbreviate this term to simply a G5-dendrimer, e.g. a 5th
generation polypropylene imine is abbreviated to a “G5-PPI-
dendrimer.”
Intermediates during the dendrimer synthesis are sometimes denoted
half-generations, a well-known example is the carboxylic acid-
terminated PAMAM dendrimers.
Diameter of dendrimer with an ethylenediamine core increases from 1.1
to 12.4 nm.
16
17. 17
PAMAM dendrimers of low generation,G0-G3, have ellipsoidal shapes.
PAMAM dendrimers of high generations,G4-G10, with well defined cavities
have roughly spherical shapes.
19. Properties Of Dendrimers
Sr.
No
Property Dendrimers Linear Polymers
1 Structure Compact, Globular Not compact
2 Synthesis Careful & stepwise
growth
Single step polycondensation
3 Structural control Very high Low
4 Architecture Regular Irregular
5 Shape Spherical Random coil
6 Aqueous
solubility
High Low
7 Nonpolar
solubility
High Low
8 Viscosity Non linear relationship
with molecular weight
Linear relation with molecular
weight
9 Reactivity High Low
10 Compressibility Low High
11 Polydispersity Monodisperse Polydisperse
19