In-vitro dissolution and microbial inhibition studies on anticancer drug etoposide with β-cyclodextrin

被引:26
|
作者
Arumugam, Shanmuga Priya [1 ]
Balakrishnan, Suganya Bharathi [1 ]
Ganesan, Vigneshkumar [1 ]
Munisamy, Maniyazagan [1 ]
Kuppu, Sakthi Velu [1 ]
Narayanan, Vimalasruthi [1 ]
Baskaralingam, Vaseeharan [2 ]
Jeyachandran, Sivakamavalli [2 ]
Thambusamy, Stalin [1 ]
机构
[1] Alagappa Univ, Sch Chem Sci, Dept Ind Chem, Karaikkudi 630003, Tamil Nadu, India
[2] Alagappa Univ, Dept Anim Hlth & Management, Karaikkudi 630003, Tamil Nadu, India
关键词
Etoposide; beta-Cyclodextrin; Phase solubility; Dissolution rate; Antimicrobial efficacy; INCLUSION COMPLEX; PHOTOPHYSICAL PROPERTIES; 2,4-DINITROBENZOIC ACID; CHEMOSENSOR PROBE; UV ABSORBER; DELIVERY; SOLUBILITY; ANTITUMOR; RELEASE; PH;
D O I
10.1016/j.msec.2019.04.033
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this article, we have reported the inclusion complex behaviors and their pharmaceutical application of anticancer drug property of Etoposide with beta-cyclodextrin. The inclusion complex is used to improve the poor aqueous solubility of the anticancer drug Etoposide. The aqueous solubility and in-vitro dissolution studies support to the anticancer drug Etoposide with beta-cyclodextrin complex is significantly improves the aqueous solubility. Etoposide: beta-cyclodextrin solid-state complexes were prepared by Physical mixture, kneading and solvent evaporation methods, and were characterized by FT-IR, (HNMR)-H-1, XRD, DSC and SEM techniques. In addition, the in-vitro antimicrobial and antibiofilm study of Etoposide drug is a sensible microorganism was significantly increased by an inclusion complexation process. The antibiofilm of anticancer drug Etoposide with ji-cyclodextrin studies have been analyzed by confocal laser scanning microscopy.
引用
收藏
页码:96 / 105
页数:10
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