Praziquantel-loaded calcite crystals: Synthesis, physicochemical characterization, and biopharmaceutical properties of inorganic biomaterials for drug delivery

方解石 碳酸钙 溶解 差示扫描量热法 材料科学 吡喹酮 药物输送 溶解试验 碳酸盐 化学工程 化学 矿物学 核化学 纳米技术 有机化学 医学 冶金 免疫学 血吸虫病 蠕虫 工程类 物理 热力学 生物制药分类系统
作者
Luisa Di Marzio,Ana Borrego‐Sánchez,Martina Felaco,MariaElena Pacinelli,Jaime Gómez‐Morales,Nicola d’Avanzo,C. Ignacio Sainz‐Díaz,Christian Celia,César Viseras
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier BV]
卷期号:68: 103021-103021 被引量:3
标识
DOI:10.1016/j.jddst.2021.103021
摘要

Drug delivery systems impacted significantly biomedical research, and the number of nano- and micro-formulations recently approved for clinical trials or marketed increased. Raw materials-based drug delivery systems have currently organic and inorganic origin, and calcium carbonate particles demonstrated several potentialities in biomedical applications and controlled drug delivery as well as they are safe and biocompatible. The aim of this study was the synthesis of calcium carbonate particles to improve the dissolution rate of praziquantel, a poorly water-soluble drug which is the gold standard for the treatment of parasite infections. Calcium carbonate particles were obtained using a synthetic carbon-based approach. Physicochemical properties of calcium carbonate particles, with or without praziquantel, were carried out by using scanning electron microscopy, Fourier transformed infrared spectroscopy, X-ray powder diffraction, thermal gravimetry and differential scanning calorimetry analysis. The solid-state characterization of calcium carbonate particles demonstrated that calcite crystals are synthesized, and these crystals interact specifically with praziquantel. The release profiles of praziquantel from calcium carbonate particles were further studied using United States Pharmacopeia dissolution test and the amount of drug released was quantified by using high performance liquid chromatography. Calcium carbonate particles increased the dissolution rate of praziquantel, which is higher than pure crystalline drug. Resulting data may suggest a potential application of these inorganic particles for oral and controlled release of praziquantel and their potential use as novel therapy for human helminthes infections. • Calcite improved the water solubility rate of Praziquantel (PZQ) in vitro. • Calcite crystals were obtained by using the carbonation process. • Morphology of resulting particles was strongly affected by synthesis' temperature. • PZQ-calcite particle interaction modified the crystal properties of pure compound.
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