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Mucoadhesive microspheres of propranolol hydrochloride for nasal delivery

Author(s): PM Dandagi, VS Mastiholimath, AP Gadad, SR Iliger
Department of Pharmaceutics, K. L. E. S's College of Pharmacy, J. N. M. C. Campus, Nehru Nagar, Belgaum - 590 010, India

Correspondence Address:
P M Dandagi Department of Pharmaceutics, K. L. E. S's College of Pharmacy, J. N. M. C. Campus, Nehru Nagar, Belgaum - 590 010 India E-mail: [email protected]

Gelatin A microspheres of propranolol hydrochloride for intranasal systemic delivery were developed with the aim to avoid first pass metabolism, to improve the patient compliance, to use an alternative therapy to conventional dosage form, to achieve controlled blood level profiles, and to improve the therapeutic efficacy of propranolol hydrochloride in the treatment of various cardiovascular disorders and as a prophylactic for migraine. Gelatin A microspheres were prepared by emulsion crosslinking method using glutaradehyde as a crosslinking agent. Gelatin and chitosan were used as polymer and co polymer respectively. All the prepared microspheres were evaluated for physical characteristics, such as particle size, incorporation efficiency, swelling index, in vitro bioadhesion using rat jejunum and in vitro drug release in pH 6.6 phosphate buffer. Average particle size of microspheres was found to be in the size range 1-50 mm. Increase in drug and polymer concentration in the formulation increased incorporation efficiency. All the microsphers showed good bioadhesive properties and swelling indices and good sustained release of drug. The data indicates that propranolol hydrochloride release followed Higuchi's matrix and Peppa's model. Stability studies showed stability of formulation at all the conditions to which they were subjected.

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