Javaid Sana, Ahmad Nasir M, Mahmood Azhar, Nasir Habib, Iqbal Mudassir, Ahmad Naveed, Irshad Sundus
School of Natural Sciences (SNS), National University of Science and Technology (NUST), Islamabad 44000, Pakistan.
Department of Chemistry, University of Wah, Wah Cantt 47040, Pakistan.
Polymers (Basel). 2021 Jun 30;13(13):2180. doi: 10.3390/polym13132180.
The objective of the present study was to achieve the successful encapsulation of a therapeutic agent to achieve antifouling functionality regarding biomedical applications. Considering nanotechnology, drug-loaded polycaprolactone (PCL)-based nanoparticles were prepared using a nano-precipitation technique by optimizing various process parameters. The resultant nano-formulations were investigated for in vitro drug release and antifouling applications. The prepared particles were characterized in terms of surface morphology and surface properties. Optimized blank and drug-loaded nanoparticles had an average size of 200 nm and 216 nm, respectively, with associated charges of -16.8 mV and -11.2 mV. Studies of the in vitro release of drug were carried out, which showed sustained release at two different pH, 5.5 and 7.4 Antifouling activity was observed against two bacterial strains, Gram-positive and Gram-negative . The zone of inhibition of the optimized polymeric drug-loaded nanoparticle F-25 against both strains were compared with the pure drug. The gradual pH-responsive release of antibiotics from the biodegradable polymeric nanoparticles could significantly increase the efficiency and pharmacokinetics of the drug as compared to the pure drug. The acquired data significantly noted that the resultant nano-encapsulation of antifouling functionality could be a promising candidate for topical drug delivery systems and skin applications.
本研究的目的是成功封装一种治疗剂,以实现生物医学应用中的防污功能。考虑到纳米技术,通过优化各种工艺参数,采用纳米沉淀技术制备了载药聚己内酯(PCL)基纳米颗粒。对所得的纳米制剂进行了体外药物释放和防污应用研究。对制备的颗粒进行了表面形态和表面性质的表征。优化后的空白纳米颗粒和载药纳米颗粒的平均粒径分别为200 nm和216 nm,相关电荷分别为-16.8 mV和-11.2 mV。进行了药物的体外释放研究,结果表明在两种不同的pH值(5.5和7.4)下均有持续释放。观察到对两种细菌菌株(革兰氏阳性菌和革兰氏阴性菌)的防污活性。将优化后的载药聚合物纳米颗粒F-25对两种菌株的抑菌圈与纯药物进行了比较。与纯药物相比,抗生素从可生物降解聚合物纳米颗粒中的逐渐pH响应释放可显著提高药物的效率和药代动力学。所获得的数据显著表明,所得的具有防污功能的纳米封装可能是局部给药系统和皮肤应用的有前途的候选者。