Son Kyoung Dan, Kim Young-Jin
Department of Biomedical Engineering, Catholic University of Daegu, Gyeongsan, 38430 Republic of Korea.
Biomater Res. 2017 Jun 24;21:13. doi: 10.1186/s40824-017-0099-1. eCollection 2017.
Calcium phosphate (CaP) based nanoparticles are considered to be ideal drug carriers for delivery of anticancer drugs because of their excellent biocompatibility and pH responsiveness. However, CaP nanoparticles have the problems of limited drug load capacity, initial burst release, and short-term release. Thus, we prepared the CaP nanocomposites containing anticancer drug such as caffeic acid (CA-NP), chlorogenic acid (CG-NP), or cisplatin (CP-NP) in the presence of alginate as a polymer template to control the release rate of drugs.
The drug-loaded CaP nanocomposites exhibited spherical shape with a size of under 100 nm and the size of nanocomposites was hardly affected by the addition of drug. UV-visible spectroscopic analysis confirmed the insertion of drug into the CaP nanocomposites. These nanocomposites showed an initial burst release of drug, followed by a prolonged release, in which the release profile of drugs was depended on the solution pH. In addition, the drug-loaded CaP nanocomposites revealed anticancer activity on human osteosarcoma in a manner dependent on concentration of drugs and time.
The drug-loaded CaP nanocomposites can contribute to the development of a new generation of controlled drug release carriers for chemotherapy of cancers.
磷酸钙(CaP)基纳米颗粒因其优异的生物相容性和pH响应性,被认为是递送抗癌药物的理想药物载体。然而,CaP纳米颗粒存在载药量有限、初始突释和短期释放等问题。因此,我们在海藻酸盐作为聚合物模板的存在下制备了含有抗癌药物如咖啡酸(CA-NP)、绿原酸(CG-NP)或顺铂(CP-NP)的CaP纳米复合材料,以控制药物的释放速率。
载药的CaP纳米复合材料呈球形,尺寸在100nm以下,纳米复合材料的尺寸几乎不受药物添加的影响。紫外可见光谱分析证实药物插入到CaP纳米复合材料中。这些纳米复合材料表现出药物的初始突释,随后是缓释,其中药物的释放曲线取决于溶液的pH值。此外,载药的CaP纳米复合材料对人骨肉瘤显示出抗癌活性,其方式取决于药物浓度和时间。
载药的CaP纳米复合材料有助于开发新一代用于癌症化疗的控释药物载体。