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Current Applied Polymer Science

Editor-in-Chief

ISSN (Print): 2452-2716
ISSN (Online): 2452-2724

Research Article

Electrically Triggered Transdermal Drug Delivery Utilizing Poly(Acrylamide)-graft-Guar Gum: Synthesis, Characterization and Formulation Development

Author(s): Ravindra P. Birajdar, Sudha S. Patil, Vijaykumar V. Alange and Raghavendra V. Kulkarni*

Volume 3, Issue 1, 2019

Page: [64 - 74] Pages: 11

DOI: 10.2174/2452271602666181031093243

Price: $65

Abstract

Objective: The study aimed to prepare electrically-triggered transdermal drug delivery systems (ETDS) using electrically responsive polyacrylamide-graft-gaur gum (PAAm-g-GaG) copolymer.

Methods: The PAAm-g-GaG copolymer was synthesized by adopting free radical polymerization grafting method. This PAAm-g-GaG copolymer hydrogel acts as a drug reservoir and blend films of Guar Gum (GaG) and Polyvinyl Alcohol (PVA) were included as Rate Controlling Membranes (RCM) in the system. The PAAm-g-GaG copolymer was characterized by FTIR, neutralization equivalent values, thermogravimetric analysis and elemental analysis.

Results: On the basis of results obtained, it is implicit that the drug permeation decreased with an increase in the concentration of glutaraldehyde and RCM thickness; while drug permeation rate was increased with increasing applied electric current strength from 2 to 8 mA. A two fold increase in flux values was observed with the application of DC electric current. An increase in drug permeation was witnessed under “on” condition of electric stimulus and permeation was decreased when electric stimulus was “off”. The skin histopathology study confirmed the changes in skin structure when electrical stimulus was applied.

Conclusion: The electrically-sensitive PAAm-g-GaG copolymer is a useful biomaterial for transdermal drug delivery application.

Keywords: Drug permeation, electrically-triggered, graft copolymer, guar gum, hydrogel, transdermal delivery systems.

Graphical Abstract

[1]
Sethi B, Mazumder R. Formulation and evaluation of transdermal patches using synthetic and natural polymers: To study release profile. Imperial J Interdisci Res 2016; 2: 15-21.
[2]
Murdan S. Electro-responsive drug delivery from hydrogels. J Control Release 2003; 92: 1-17.
[3]
Karande P, Mitragotri S. Enhancement of transdermal drug delivery via synergistic action of chemicals. Biochim Biophys Acta 2009; 1788: 2362-73.
[4]
Darwhekar G, Jain D, Patidar V. Formulation and evaluation of transdermal drug delivery system of clopidogrel bisulfate. Asian J Pharm Life Sci 2011; 1: 269-75.
[5]
Bhattacharya A, Misra BN. Grafting: A versatile means to modify polymers techniques, factors and applications. Progress in Prog Polym Sci 2004; 29: 767-814.
[6]
Kulkarni RV, Sa B. Electrically responsive smart hydrogels in drug delivery: A review. J Appl Biomater Biomech 2007; 5: 125-39.
[7]
Pucci V, Mandrioli R, Ferranti A, Furlanetto S, Raggi MA. Quality control of commercial tablets containing the novel antipsychotic quetiapine. J Pharm Biomed Anal 2003; 32: 1037-44.
[8]
Gawali P, Gupta A, Kachare S, Kshirsagar S. Formulation and evaluation of matrix-based sustained release tablets of quetiapine fumarate and the influence of excipients on drug release. J Chem Pharm Res 2012; 4: 3073-81.
[9]
Kulkarni RV, Sa B. Enteric delivery of ketoprofen through functionally modified poly(acrylamide-grafted-xanthan) based pH-sensitive hydrogel beads: Preparation, in-vitro and in-vivo evaluation. J Drug Target 2008; 16: 167-77.
[10]
Tripathy T, Singh RP. High performance flocculating agent based on partially hydrolysed sodium alginate-g-polyacrylamide. Eur Polym J 2000; 36: 1471-6.
[11]
Mutalik S, Udupa N. Formulation development, in vitro and in vivo evaluation of membrane controlled transdermal systems of glibenclamide. J Pharm Pharm Sci 2005; 8: 26-38.
[12]
Pillai O, Panchagula R. Transdermal delivery of insulin from poloxamer gel: Ex vivo and in vivo skin permeation studies in rat using iontophoresis and chemical enhancers. J Control Release 2003; 89: 127-40.
[13]
Kulkarni RV, Setty CM, Sa B. Polyacrylamide-g-alginate-based electrically responsive hydrogel for drug delivery application: Synthesis, characterization, and formulation development. J Appl Polym Sci 2010; 115: 1180-8.
[14]
Soppimath KS, Kulkarni AR, Aminabhavi TM. Chemically modified polyacrylamide-grafted-guar gum based crosslinked anionic microgels as pH-sensitive drug delivery systems: Preparation and characterization. J Control Release 2001; 75: 331-45.
[15]
Chattopadhyay A. Studies on guar gum-graft-acrylamide: Characterization and polyvalent metal ion binding. Int J Chem Studies 2015; 2(6): 5-8.
[16]
Rathore K, Loonker S. Synthesis, characterization and swelling behaviour of guar gum-g-poly (methyl methacrylate) superabsorbent nanocomposite. Asian J Chem Sci 2017; 2(1): 1-13.
[17]
Alange VV, Birajdar RP, Kulkarni RV. Functionally modified polyacrylamide-graft-gum karaya pH-sensitive spray dried microspheres for colon targeting of an anti-cancer drug. Int J Biol Macromol 2017; 102: 829-39.
[18]
Kulkarni RV, Wagh YJ. Crosslinked alginate films as rate controlling membranes for transdermal drug delivery application. J Macromol Sci Part A Pure Appl Chem 2010; 47: 732-7.
[19]
Kulkarni RV, Sa B. Electroresponsive polyacrylamide-grafted-xanthan hydrogels for drug delivery. J Bioact Compat Polym 2009; 24: 368-84.

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