A NOVEL VESICULAR APPROACH FOR TRANSDERMAL ADMINISTRATION OF ENALAPRIL MALEATE LOADED NANOPRONIOSOMAL GEL: FORMULATION, EX VIVO EVALUATION AND IN VIVO ANTIHYPERTENSIVE STUDY

  • M. SABAREESH Jawaharlal Nehru Technological University Anantapur, Ananthapuramu, Andhra Pradesh, India
  • J. P. YANADAIAH Department of Pharmacognosy, Dr. K. V. Subba Reddy Institute of Pharmacy, Kurnool, Andhra Pradesh, India
  • K. B. CHANDRA SEKHAR Department of Chemistry, Krishna University, Machilipatnam, Andhra Pradesh, India

Abstract

Objective: The objective of the study was to formulate and evaluate the nanoproniosomal gel of Enalapril maleate (EM) for the treatment of hypertension through the transdermal administration and to provide better bioavailability.


Methods: The nanoproniosomal gel of the EM was formulated by Lecithin, Cholesterol, Non-ionic surfactants using the Coacervation-phase separation method. The prepared nanoproniosomal gels were evaluated for pH and viscosity, vesicle size analysis, rate of spontaneity, entrapment efficiency, zeta potential, ex vivo skin permeation studies, skin irritation test, stability studies and in vivo antihypertensive studies.


Results: Physical characterization was found to be within acceptable limits. The ex vivo skin permeation studies showed the cumulative permeation of 58.75 % to 89.72 % through the albino rat skin in 24 h for all the formulations, which indicate the zero-order drug permeation with diffusion, non-fickian release. Among all formulations, EMNP7 was selected as best formulation because it showed better characteristics than other formulations in several aspects like physicochemical characterization, ex vivo skin permeation studies, permeation kinetics, and other evaluation parameters. The skin irritation study revealed that there was no irritation after topical application and it was found to be safer to use. The In vivo antihypertensive study revealed that the formulation of EMNP7 was successful to regress the rat blood pressure (BP) to normal values in experimental hypertensive rats.


Conclusion: The nanoproniosomal gel is an efficient transdermal therapeutic system for the delivery of EM for the treatment of hypertension. It is suitable for once a day controlled release formulation.

Keywords: Cholesterol, Enalapril maleate, Ex vivo Permeation studies, In vivo antihypertensive studies, Lecithin, Nonionic surfactants, Proniosomes, Skin irritation studies, Transdermal gel

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SABAREESH, M., YANADAIAH, J. P., & SEKHAR, K. B. C. (2020). A NOVEL VESICULAR APPROACH FOR TRANSDERMAL ADMINISTRATION OF ENALAPRIL MALEATE LOADED NANOPRONIOSOMAL GEL: FORMULATION, EX VIVO EVALUATION AND IN VIVO ANTIHYPERTENSIVE STUDY. International Journal of Applied Pharmaceutics, 12(5), 190-202. https://doi.org/10.22159/ijap.2020v12i5.38463
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