Ullah Farhad, Iqbal Zafar, Khan Amjad, Khan Saeed Ahmad, Ahmad Lateef, Alotaibi Amal, Ullah Riaz, Shafique Muhammad
Department of Pharmacy, University of Peshawar, Peshawar, Pakistan.
Department of Pharmacy, Kohat University of Science and Technology (KUST), Kohat, Pakistan.
Front Pharmacol. 2022 Jun 30;13:911771. doi: 10.3389/fphar.2022.911771. eCollection 2022.
Oral administration of pH sensitive/stimuli responsive nanoparticles are gaining importance because of the limited side effects, minimum dose and controlled drug release. The objective of this study was to develop and evaluate pH sensitive polymeric nanoparticles for methotrexate with the aim to maximize the drug release at target site. In the presented study, pH sensitive polymeric nanoparticles of methotrexate were developed through modified solvent evaporation technique using polymer Eudragit S100. Different process parameters like drug to polymer ratio, speed of sonication, concentration of surfactant and time of sonication were optimized by evaluating their effects on particle size, PDI, zeta potential, entrapment/encapsulation efficiency. The developed formulations were evaluated for their size, polydispersity (PDI), zeta potential, encapsulation efficiency, XRD, scanning electron microscopy, drug release and stability studies. Best results were obtained with poloxamer-407 and PVA and were selected as surfactants. Physicochemical characterization of the developed formulations showed that the particle size lies in the range 165.7 ± 1.85-330.4 ± 4.19, PDI 0.119 ± 0.02-0.235 ± 0.008, zeta potential -0.163 ± 0.11--5.64 ± 0.36 mV, and encapsulation efficiency more than 61%. The results of scanning electron microscopy revealed that nanoparticles have regular geometry with spherical shape. Initially the drug release occur through diffusion followed by erosion. The present studies showed that MTX-ES100 nanoparticles prepared during this study have the desired physicochemical properties, surface morphology and release characteristics used to target the desired organs.
由于副作用有限、剂量最小且药物释放可控,口服pH敏感/刺激响应性纳米颗粒正变得越来越重要。本研究的目的是开发和评估用于甲氨蝶呤的pH敏感聚合物纳米颗粒,以使药物在靶部位的释放最大化。在本研究中,通过使用聚合物Eudragit S100的改良溶剂蒸发技术制备了甲氨蝶呤的pH敏感聚合物纳米颗粒。通过评估药物与聚合物比例、超声速度、表面活性剂浓度和超声时间等不同工艺参数对粒径、多分散指数(PDI)、zeta电位、包封/封装效率的影响,对其进行了优化。对所开发的制剂进行了粒径、多分散性(PDI)、zeta电位、封装效率、X射线衍射(XRD)、扫描电子显微镜、药物释放和稳定性研究。使用泊洛沙姆-407和聚乙烯醇(PVA)获得了最佳结果,并将其选作表面活性剂。所开发制剂的物理化学表征表明,粒径范围为165.7±1.85 - 330.4±4.19,PDI为0.119±0.02 - 0.235±0.008,zeta电位为-0.163±0.11 - -5.64±0.36 mV,封装效率超过61%。扫描电子显微镜结果显示,纳米颗粒具有规则的几何形状且呈球形。最初,药物释放通过扩散发生,随后是侵蚀。本研究表明,本研究期间制备的MTX-ES100纳米颗粒具有用于靶向所需器官的理想物理化学性质、表面形态和释放特性。