The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System
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The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System
The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System
Chinese Journal of Polymer Science2014年32卷第12期 页码:1714-1723
Affiliations:
a.School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China
b.Information Center, China Food and Drug Administration, Beijing 100053, China
c.Graduate School of Frontier Science, University of Tokyo, Chiba 277-8561, Japan
Author bio:
**Lin Ye (叶霖), E-mail: yelin@bit.edu.cn
Funds:
National Undergraduate Training Programs for Innovation and Entrepreneurship(201310007048);Basic Research Foundation of Beijing Institute of Technology(20120942005);This work was financially supported by the National Natural Science Foundation of China(21104005)
Yang Hu, Lu Gan, Qian-xuan Li, 等. The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System[J]. Chinese Journal of Polymer Science, 2014,32(12):1714-1723.
Yang Hu, Lu Gan, Qian-xuan Li, et al. The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System[J]. Chinese Journal of Polymer Science, 2014, 32(12): 1714-1723.
Yang Hu, Lu Gan, Qian-xuan Li, 等. The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System[J]. Chinese Journal of Polymer Science, 2014,32(12):1714-1723.DOI: 10.1007/s10118-014-1542-6.
Yang Hu, Lu Gan, Qian-xuan Li, et al. The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System[J]. Chinese Journal of Polymer Science, 2014, 32(12): 1714-1723.DOI: 10.1007/s10118-014-1542-6.
The Preparation of Cationic Folic Acid and Its Application in Drug Delivery System
The cationic folic acid (CFA) was prepared by introducing triethylenetetramine into folic acid with EDCI/NHS and characterized by IR
NMR and mass spectra. It was found that approximately one of two carboxyls in the folic acid molecule was substituted to form CFA. The conversion of
γ
-carboxyl is found to be 59% higher than 30% of
α
-carboxyl. The CFA and doxorubicin hydrochloride can be loaded on the ionic shell of PTX-encapsulated micelle to form CFA loaded binary drug carrier
via
static interaction in aqueous solutions. The successful loading was demonstrated by zeta potential measurement and the drug load amount (DLA) of CFA was measured by HPLC.
In vitro
cytotoxicity results revealed the CFA drug carrier showed higher cytotoxicity to cancer cell MDA-MB-321 than the binary drug carrier without CFA and the positive control
while it showed lower cytotoxicity to normal cell HUVEC than the positive control
and similar cytotoxicity with the binary drug carrier without CFA. These results as well as confocal laser scanning microscopy observation indicate the synthesized CFA drug carrier possesses active tumor-targeting property.
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