OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER
Abdalla, R., Mahdy, M., Abd-Rahman, M., Megrab, N. (2001). OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER. EKB Journal Management System, 10(2), 30-35. doi: 10.21608/zjps.2001.181585
Ramadan Abdalla; Mahmoud Mahdy; Mohamed Abd-Rahman; Nagia Megrab. "OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER". EKB Journal Management System, 10, 2, 2001, 30-35. doi: 10.21608/zjps.2001.181585
Abdalla, R., Mahdy, M., Abd-Rahman, M., Megrab, N. (2001). 'OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER', EKB Journal Management System, 10(2), pp. 30-35. doi: 10.21608/zjps.2001.181585
Abdalla, R., Mahdy, M., Abd-Rahman, M., Megrab, N. OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER. EKB Journal Management System, 2001; 10(2): 30-35. doi: 10.21608/zjps.2001.181585

OCULAR CONTROLLED DELIVERY OF BRIMONIDINE USING LIPOSOMES AS A PARTICULATE CARRIER

Zagazig Journal of Pharmaceutical Sciences
Article 6, Volume 10, Issue 2, December 2001, Page 30-35  XML PDF (2.88 MB)
Document Type: Original Article
DOI: 10.21608/zjps.2001.181585
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Authors
Ramadan Abdalla email 1; Mahmoud Mahdy2; Mohamed Abd-Rahman2; Nagia Megrab3
1Department of Ophthalmology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
2Department of Pharmaceutics, Faculty of pharmacy, Zagazig University, Faculty of Pharmacy, Suez Canal University, Egypt.
3Department of Pharmaceutics, Faculty of Pharmacy, Suez Canal University, Egypt
Abstract
The ocular activity of a single dose of brimonidine o.2 % in solution and liposomal formulations was evaluated in 28 adult patients with recently diagnosed primary open angle glaucoma. Multilamellar liposomes were prepared from dipalmitoyl phosphatidcholine and cholesterol. Stearylamine and dicetyl phosphate were used to modify the net surface charge of liposomes. The evaluation of the performance of various formulations of the drug was assessed on the basis of the influence of the drug on the intraocular pressure. Results demonstrated that the intra-ocular activity of the drug using various liposomal formulations was greater than that of solution form. Moreover, concerning the liposomal surface charge, the drug activity was greatest for positively charged liposomes, less for neutral liposomes and least for negatively charged liposomes. This could be attributed to electrostatic attraction between the negatively charged surface of the corneal epithelial and positively charged liposomal surface.
In conclusion, it was clearly observed that liposomal ophthalmic drug delivery system seems to be a promising approach for the selective targeting of the drug.
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