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Anti - oxidant coated liposome as the delivery system for papain based natural cosmetics

脂质体 透皮 木瓜蛋白酶 纳米载体 卵磷脂 化学 磷脂酰胆碱 色谱法 药物输送 药理学 有机化学 生物化学 磷脂 膜 酶 医学
作者
Nur Zatul Iradah Roslan,Azila Abdul Aziz,Mohammad Roji Sarmidi,Ramlan Aziz
标识
DOI:10.1109/escinano.2010.5700962
摘要

Liposome is a topical delivery system that has evoked a considerable interest in the cosmetic industry. Liposome is biocompatible, biodegradable, exhibits low toxicity and has the ability to entrap both hydrophilic and lipophilic active materials [1]. Over the last decades, liposome has been intensively studied as nanocarriers for transdermal administration of drugs and skin care active ingredients [2]. Papain, a protease, is an exfoliating agent which has also been touted to be able to reduce the signs of aging. In this study, liposome was used to enhance the transdermal penetration of papain into the skin [2]. In addition, liposome also stabilizes papain and reduces skin damage due to direct exposure to papain. Liposome can be formed from pure L-a-phosphatidylcholine or from cheaper sources such as soybean lecithin. However, liposome from soybean lecithin can be oxidized easily due to its unsaturated fatty acid chains. To overcome this problem, in this work antioxidant was added to decrease liposome oxidation and thus increase stability. The liposome, which was at pH 6.5, was stored at 25°C and 4°C and the stability of the liposome was monitored up to sixty days. Coated liposome was found to be more stable than uncoated liposome regardless of storage temperature. After two months, the encapsulation efficiency of the coated liposome was approximately 80%, whilst the encapsulation efficiency of the uncoated liposome was approximately 74%. Percutaneous penetration study was conducted to assess the efficiency of the transdermal delivery of the liposome-papain through the skin. Results obtained from the analysis showed that liposome-papain effectively penetrated the skin. Various studies have suggested that liposome increases percutaneous penetration of compounds through interaction of vesicles with the stratum corneum [3] and that this penetration is responsible for the greater concentration of the active ingredient in the skin.
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