Abstract
Two types of amphoteric calix[n]arene carboxylic acid (CnCA) derivative, i.e., calix[6]arene hexa-carboxylic acid (C 6 HCA) and calix[8]arene octo-carboxylic acid (C 8OCA), were synthesized by introducing acetoxyls into the hydroxyls of calix[n]arene (n-6, 8). C6HCA and C8 OCA nanoparticles (NPs) were prepared successfully using the dialysis method. C nCA NPs had regular spherical shapes with an average diameter of 180-220 nm and possessed negative charges of greater than -30 mV. C6 HCA and C8OCA NPs were stable in 4.5% bovine serum albumin solutions and buffers (pH 5-9), with a low critical aggregation concentration value of 5.7 mg•L--1 and 4.0 mg•L--1, respectively. C6 HCA and C8 OCA NPs exhibited good paclitaxel (PTX) loading capacity, with drug loading contents of 7.5% and 8.3%, respectively. The overall in vitro release behavior of PTX from the CnCA NPs was sustained, and C 8 OCA NPs had a slower release rate compared with C6 HCA NPs. These favorable properties of CnCA NPs make them promising nanocarriers for tumortargeted drug delivery.
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Zhao, Z. M., Wang, Y., Han, J., Zhu, H. D., & An, L. (2015). Preparation and characterization of amphiphilic calixarene nanoparticles as delivery carriers for paclitaxel. Chemical and Pharmaceutical Bulletin, 63(3), 180–186. https://doi.org/10.1248/cpb.c14-00699
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