scholarly journals DESIGN AND CHARACTERIZATION OF UNIDIRECTIONAL DRUG RELEASE OF METFORMIN HYDROCHLORIDE USING TRANSDERMAL DRUG DELIVERY SYSTEM

2014 ◽  
Vol 01 (02) ◽  
pp. 41-46
Author(s):  
SOWJANYA BATTU ◽  
UMA MAHESHWAR R VATIKUTI
Author(s):  
DIPJYOTI BISWAS ◽  
SUDIP DAS ◽  
SOURAV MOHANTO ◽  
SHUBHRAJIT MANTRY

The modified/regulated drug delivery system helps to sustain the delivery of the drug for a prolonged period. The modified drug delivery system is primarily aimed at ensuring protection, the effectiveness of the drug, and patient compliance. The transdermal drug delivery system (TDDS) falls within the modified drug delivery system, in which the goal is to deliver the drug at a fixed dose and regulated rate through the skin. Polymers are the backbone of the framework for providing transdermal systems. The polymer should be stable, non-toxic, economical, and provide a sustainable release of the drug. In general, natural polymers used in the TDDS as rate-controlling agents, protective, and stabilizing agents and also used to minimize the frequency of dosing and improve the drug’s effectiveness by localizing at the site of action. Nowadays, manufacturers are likely to use natural polymers due to many issues associated with drug release and side effects with synthetic polymers. Drug release processes from natural polymers include oxidation, diffusion, and swelling. Natural polymers may be used as the basis to achieve predetermined drug distribution throughout the body. The use of natural materials for traditional and modern types of dosage forms are gums, mucilages, resins, and plant waste etc. Thus, the main objective of this review article is to give a brief knowledge about the extraction, modification, characterization, and biomedical application of conventional natural polymers used in the transdermal drug delivery system and their future prospective.


2016 ◽  
Vol 7 (1) ◽  
pp. 66-76 ◽  
Author(s):  
Venkata Ramana Malipeddi ◽  
Rajendra Awasthi ◽  
Daniela Dal Molim Ghisleni ◽  
Marina de Souza Braga ◽  
Irene Satiko Kikuchi ◽  
...  

Author(s):  
Subramanian S ◽  
Senith SK

Transdermal drug delivery is an alternative route for systemic drug delivery which minimizes the absorption and increases the bioavailability. Orally clopidogrel bisulfate has a short elimination half-life (7-8 h), low oral bioavailability (50 %) undergoes extensive first pass metabolism (85 %) and frequent high doses (75 mg) are required to maintain the therapeutic level as a result. The purpose of this research was formulation and evaluation of transdermal drug delivery system of clopidogrel bisulfate using various polymers such as HPMC and EC by solvent casting technique for improvement of bioavailability of drug and reducing toxic effects. The developed transdermal patches may increase the therapeutic efficacy and reduce toxic effect of clopidogrel bisulfate. The prepared transdermal drug delivery system of clopidogrel bisulfate using different polymers such as HPMC and EC had shown good & promising results for all the evaluated parameters. Based on the in vitro drug release, drug content, weight variation, tensile strength, thickness and folding endurance results formulation F2 was concluded as an optimized formulation which shows its higher percentage of drug release. Keyword: Clopidogrel bisulfate; Transdermal patch; TDDS; Solvent evaporation; In vitro drug release


Soft Matter ◽  
2019 ◽  
Vol 15 (41) ◽  
pp. 8361-8371 ◽  
Author(s):  
Ke Peng ◽  
Thomas Sottmann ◽  
Cosima Stubenrauch

First formulation and characterization of a non-toxic bicontinuous microemulsion gelled by a molecular gelator as potential transdermal drug delivery system.


Sign in / Sign up

Export Citation Format

Share Document