Amphiphilic Block Copolymers: A Novel Substance for Bitter-Masking in Aqueous Solutions

被引:12
|
作者
Li, Pan [1 ]
Tian, Yin [1 ]
Ke, Xiu-Mei [1 ]
Tan, Qing-Chu [1 ]
Han, Xue [3 ]
Ma, Hong-Yan [1 ]
Pei, Jin [1 ]
Lin, Jun-Zhi [4 ]
Xu, Run-Chun [1 ]
Han, Li [1 ]
Yang, Ming [2 ]
Zhang, Ding-Kun [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, State Key Lab Breeding Base Systemat Res Dev & Ut, Chengdu 611137, Peoples R China
[2] Jiangxi Univ Tradit Chinese Med, Nanchang 330004, Jiangxi, Peoples R China
[3] Chengdu Med Coll, Shool Pharm, Chengdu 610083, Peoples R China
[4] Chengdu Univ Tradit Chinese Med, Teaching Hosp, Cent Lab, Chengdu 610072, Peoples R China
基金
中国国家自然科学基金;
关键词
amphiphilic block copolymers; bitter-masking; bitter receptors; self-assembled micelles; pharmaceutics principle; HOT-MELT EXTRUSION; TASTE MASKING; PREDICTION; ENERGIES; MICELLES; CHILDREN; DELIVERY; POLYMER; TABLETS; QUININE;
D O I
10.1021/acs.molpharmaceut.9b01296
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
It is a challenging task to suppress the bitterness of liquid preparations, especially for children. Bitter molecules are highly dispersible in liquids, leading to a strong and instant stimulation of the bitter receptors. At present, there is no effective way to correct this issue except for adding sweeteners, resulting in an unsatisfying taste. Based on the three-point contact theory, which is a universally accepted mechanism of bitterness formation, a new idea and application of amphiphilic block copolymers (ABCs) for bitterness suppression was proposed for the first time. We found that ABCs could widely inhibit the bitterness of four typical bitter substances. The mechanism is that ABCs self-assemble to form association colloids, which attract bitter components and reduce their distribution in the molecular form in solution. The bitter components were demonstrated to automatically embed in the spiral hydrophobic cavity of the hydrophobic chain of the ABCs, and their special interaction dispersed the positive electrostatic potential of bitter groups. The combination did not affect the pharmacokinetic parameters and pharmacodynamics of bitter drugs. These findings highlight the novel application of ABCs for the inhibition of bitterness and illuminate the underlying inhibition mechanisms.
引用
收藏
页码:1586 / 1595
页数:10
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