姜黄素
生物利用度
胡椒碱
药理学
纳米载体
化学
药代动力学
体内
壳聚糖
乳状液
药物输送
医学
生物化学
有机化学
生物技术
生物
作者
Raffaele Vecchione,Vincenzo Quagliariello,Dominic Calabria,Vincenzo Calcagno,Elisa De Luca,Rosario V. Iaffaioli,Paolo A. Netti
标识
DOI:10.1016/j.jconrel.2016.05.004
摘要
Although nanocarriers can enhance the bioavailability of free curcumin in the blood, a systematic study on the parameters that affect such enhancement is still missing. In this work we focused the attention on a nanocarrier represented by an oil in water nano-emulsion coated with a thiol modified chitosan and carried out a comprehensive study on the effects that parameters such as size, co-delivery of piperine and degree of chitosan modification can exert on curcumin bioavailability and quantified their impact. We obtained an unprecedented pharmacokinetic profile of curcumin with the best formulation, represented by a combination of a small nano-emulsion size (110 nm), co-delivery of curcumin and piperine (weight ratio 100:1) and a high degree of chitosan thiolation (14–15%). Then, we assessed its anti-inflammatory properties after oral administration in rats at low doses (≤ 0.1 times the volume administered in the pharmacokinetic study). Furthermore, the proposed food grade nano-emulsions loaded with curcumin did not show any cytotoxic effect on normal fibroblasts, while they were able to promote death in colon cancer cells in agreement with the common knowledge of the selective action of curcumin.
科研通智能强力驱动
Strongly Powered by AbleSci AI