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Al-Azhar Journal of Pharmaceutical Sciences
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Volume Volume 63 (2021)
Issue Issue 1
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Kassem, A. (2021). A STUDY ON THE ROLE OF ZWITTERIONIC PHOSPHATIDYLCHOLINE LIPID (S) IN PHYSICOCHEMICAL FEATURES OF LIPOSOME ENCAPSULATED PACLITAXEL AS A DRUG DELIVERY SYSTEM. Al-Azhar Journal of Pharmaceutical Sciences, 63(1), 1-16. doi: 10.21608/ajps.2021.153554
Abdulsalam Kassem. "A STUDY ON THE ROLE OF ZWITTERIONIC PHOSPHATIDYLCHOLINE LIPID (S) IN PHYSICOCHEMICAL FEATURES OF LIPOSOME ENCAPSULATED PACLITAXEL AS A DRUG DELIVERY SYSTEM". Al-Azhar Journal of Pharmaceutical Sciences, 63, 1, 2021, 1-16. doi: 10.21608/ajps.2021.153554
Kassem, A. (2021). 'A STUDY ON THE ROLE OF ZWITTERIONIC PHOSPHATIDYLCHOLINE LIPID (S) IN PHYSICOCHEMICAL FEATURES OF LIPOSOME ENCAPSULATED PACLITAXEL AS A DRUG DELIVERY SYSTEM', Al-Azhar Journal of Pharmaceutical Sciences, 63(1), pp. 1-16. doi: 10.21608/ajps.2021.153554
Kassem, A. A STUDY ON THE ROLE OF ZWITTERIONIC PHOSPHATIDYLCHOLINE LIPID (S) IN PHYSICOCHEMICAL FEATURES OF LIPOSOME ENCAPSULATED PACLITAXEL AS A DRUG DELIVERY SYSTEM. Al-Azhar Journal of Pharmaceutical Sciences, 2021; 63(1): 1-16. doi: 10.21608/ajps.2021.153554

A STUDY ON THE ROLE OF ZWITTERIONIC PHOSPHATIDYLCHOLINE LIPID (S) IN PHYSICOCHEMICAL FEATURES OF LIPOSOME ENCAPSULATED PACLITAXEL AS A DRUG DELIVERY SYSTEM

Article 1, Volume 63, Issue 1, March 2021, Page 1-16  XML PDF (911.77 K)
Document Type: Original Article
DOI: 10.21608/ajps.2021.153554
Author
Abdulsalam Kassem
1Department of Molecular Physical Pharmaceutics, Institute of Biomedical Sciences, Tokushima University, 1–78–1 Sho-machi, Tokushima 770–8505, Japan.
Abstract
The lipid composition of the liposomal membrane plays a crucial role in the physical and pharmacological behaviors of liposomal payloads, and it can be tailored to achieve the desired delivery needs. Thus, the aim of the current study was to develop and optimize paclitaxel (PTX) loaded liposome nanocarrier using a thin-film rehydrating method and studying the influence of different zwitterionic Phosphatidylcholine (PC)  lipids with different acyl chains, on the physicochemical properties of the developed PTX liposomal formulations. The studied PC were dipalmitoyl (DPPC), dimyristoyl (DMPC) and palmitoyl-oleoyl (POPC) PCs, in combination with cholesterol. Several characteristics were monitored, including PTX entrapment efficiency (EE) of liposomes, particle size (PS), polydispersity index (PDI), zeta potential (ZP), PTX release in phosphate buffered saline (PBS) with 0.1 tween® 80 and in PBS / 10 % fetal bovine serum (FBS) cell culture medium, as well as in vitro antitumoral and therapeutic effects. The results demonstrated that DPPC exhibited superiority in the physicochemical properties when compared with DMPC and POPC. The in vitro cytotoxicity findings indicate that the PTX-liposome would be a promising substitutional approach for Taxol® as a commercial product with a toxic solvent. The results outcomes indicated that the developed PTX-liposome would be a viable drug delivery system with sustaining effect for management of colorectal cancer cells and further clinical use.
Keywords
Liposome; Paclitaxel; Cholesterol; zwitterionic Phosphatidylcholine; sustained release
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