Effect of Curcumin-Hydroxypropyl-\(\beta\)-Cyclodextrin Complex and the Complex Loaded Gelatin Carrageenan Microparticles on the Various Chemical and Biological Properties

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Bably Khatun, Munmi Majumder, R. Mukhopadhyay, Rafika Yasmin, Robin Doley, T. K. Maji
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引用次数: 1

Abstract

Curcumin was modified with 2-hydroxypropyl-\(\beta\)-cyclodextrin (HP\(\beta\)CD) to enhance its bioavailability. The modified curcumin was loaded into gelatin-carrageenan microparticles to control the drug release behavior. The different analytical techniques like Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy (RS), X-ray diffractometry (XRD), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) indicated the formation of the samples. The solubility of the modified curcumin was checked visibly and by using UV-VIS spectroscopy & optical microscopy as well. The effect of surfactant on process yield, drug loading & encapsulation efficiency, swelling and drug release from the microparticles was checked. The samples exhibited more swelling and hence drug release was more in basic compared to acidic medium and the percentage increased with increase in time. The modified curcumin, on examining in both breast and lung cancer cell lines, manifested better anticancer activity compared to curcumin as evidenced by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay, clonogenic assay and apoptosis assay. However, the microparticles didn’t reveal better anticancer activities compared to curcumin and modified curcumin. Further, all the prepared samples were found to be non-toxic to human peripheral blood mononuclear cells (PBMCs) and red blood cells (RBCs).

Abstract Image

姜黄素-羟丙基- \(\beta\) -环糊精配合物及其负载明胶卡拉胶微粒对各种化学和生物特性的影响
采用2-羟丙基- \(\beta\) -环糊精(HP \(\beta\) CD)对姜黄素进行改性,提高其生物利用度。将改性后的姜黄素装入明胶-卡拉胶微粒中,以控制药物的释放行为。傅里叶变换红外光谱(FTIR)、拉曼光谱(RS)、x射线衍射(XRD)、差示扫描量热法(DSC)、扫描电子显微镜(SEM)等不同的分析技术表明了样品的形成。用紫外-可见光谱法测定了改性后姜黄素的溶解度;还有光学显微镜。表面活性剂对工艺收率、载药量的影响考察了微颗粒的包封率、溶胀和药物释放情况。样品在碱性介质中比酸性介质中溶胀更大,因此药物释放更多,并且随时间的增加而增加。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)试验、克隆实验和细胞凋亡实验证明,改性后的姜黄素在乳腺癌和肺癌细胞系中表现出比姜黄素更好的抗癌活性。然而,与姜黄素和改性姜黄素相比,微颗粒并没有显示出更好的抗癌活性。此外,所有制备的样品都被发现对人外周血单个核细胞(PBMCs)和红细胞(rbc)无毒。
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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