Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride
Khaled, K., El-Sayed, Y., Al-Bawardi, I. (2001). Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride. EKB Journal Management System, 24(1), 65-71. doi: 10.21608/bfsa.2001.65901
K. A. Khaled; Y. M. El-Sayed; I. S. Al-Bawardi. "Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride". EKB Journal Management System, 24, 1, 2001, 65-71. doi: 10.21608/bfsa.2001.65901
Khaled, K., El-Sayed, Y., Al-Bawardi, I. (2001). 'Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride', EKB Journal Management System, 24(1), pp. 65-71. doi: 10.21608/bfsa.2001.65901
Khaled, K., El-Sayed, Y., Al-Bawardi, I. Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride. EKB Journal Management System, 2001; 24(1): 65-71. doi: 10.21608/bfsa.2001.65901

Effects of formulations and penetration enhancers on the diffusional parameters for the percutaneous absorption of propranolol hydrochloride

Bulletin of Pharmaceutical Sciences Assiut University
Article 9, Volume 24, Issue 1, June 2001, Page 65-71  XML PDF (234.85 K)
Document Type: Original Article
DOI: 10.21608/bfsa.2001.65901
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Authors
K. A. Khaled1; Y. M. El-Sayed2; I. S. Al-Bawardi2
1Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Egypt
2Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia
Abstract
Propranolol hydrochloride, the com. available form of propranolol, was formulated as gels using different cellulose polymers viz. methylcellulose, CM-​cellulose, and hydroxypropyl methylcellulose (HPMC)​.  In vitro percutaneous absorption study of the gels was conducted using improved franz diffusion cells and rabbit skin as a membrane.  The highest extent of drug penetration was obtained upon using HPMC gel formulation.  Therefore, the influence of drug concn. on its percutaneous absorption was investigated utilizing HPMC gel formulation.  The extent of drug percutaneous absorption was found to increase as drug concn. increases.  Anal. of the diffusional parameters, govern the skin penetration process, revealed that diffusion coeff. of the drug did not change as drug concn. varies.  On the other hand, the apparent permeability coeff., and the apparent partition coeff., showed dependency on drug concn.  The limit value of the partition coeff. was detd., graphically, and found to be 0.2411.  The influence of skin penetration enhancers, such as Azone, n-​decyl alc., and 1,​8-​cineol, on the percutaneous absorption of the drug was studied.  An overall low enhancing effect (max. of 5.7-​fold compared to a control) was obtained using 1,​8-​cineol.  This finding was attributed to the opposite influence of the cited enhancers on the diffusion coeff. and the partition coeff. of the drug.  The enhancers increase the resistance of the skin to the penetration of drug mols. (decreasing the diffusion coeff.)​.  Meanwhile, the enhancers facilitate the partitioning process of the drug mols. from the gel to the skin as the apparent partition coeff. increases.
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