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Original Research Article | OPEN ACCESS

Mucoadhesive carbamazepine gel for in situ olfactory delivery

Madhuri V Gaikwad1 , Sangeeta H Sahasrabuddhe2, Prashant K Puranik3

1Department of Pharmaceutics, Konkan Gyanpeeth Rahul Dharkar College of Pharmacy and Research Institute, Vengaon road, Dahiwali, Karjat 410201; 2Department of Cosmetic Technology, LAD and SMT RP College, Seminary Hills, Nagpur 440006; 3Department of Pharmaceutical Sciences, RTM Nagpur University, Nagpur 440001, Maharashtra, India.

For correspondence:-  Madhuri Gaikwad   Email: madhugaikwad09@gmail.com   Tel:+918419999379

Accepted: 25 July 2019        Published: 27 August 2019

Citation: Gaikwad MV, Sahasrabuddhe SH, Puranik PK. Mucoadhesive carbamazepine gel for in situ olfactory delivery. Trop J Pharm Res 2019; 18(8):1571-1579 doi: 10.4314/tjpr.v18i8.1

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To formulate mucoadhesive carbamazepine gel for delivery to the brain via the olfactory mucosa.
Methods: Carbamazepine transfersomes were formulated using Lipoid S 100 and sodium cholate. The transfersomes were evaluated for entrapment efficiency, in vitro release transmission electron microscopy, zeta potential, polydispersity index .The transfersomes were then incorporated into gellan gum gel, and the in situ gel formulation was evaluated for drug content, gel strength, in vitro release and mucoadhesive force. Transfersomes were also evaluated for bioanalytical study in rats.
Result: TEM analysis showed good regular spheres. The negative zeta potential ensures resistance to aggregation. The gel strength of the formulations was in the range of 0.6 to 7.4 g. In vitro diffusion study of transfersomal gel showed Fickian diffusion mechanism. Formulation F6 was optimized depending for gel strength (6.4 g) , drug content (99.47 ± 0.25 %), and good mucoadhesive force (50.24 ± 0.76 dyne/cm2).Bioanalytical study of F6 showed increased drug concentration in brain.
Conclusion: Mucoadhesive carbanmazepine gel can be used effectively to achieve increased concentration of drug  in the brain via olfactory mucosal route.

Keywords: Olfactory delivery, Carbamazepine, In situ gel Bioanalytical study

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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