Pluronic F-127辅助卡铂立方体体的制备及评价

IF 0.8 4区 医学 Q3 EDUCATION, SCIENTIFIC DISCIPLINES Indian Journal of Pharmaceutical Education and Research Pub Date : 2023-10-04 DOI:10.5530/ijper.57.4.150
Jawaher Abdullah Alamoudi, Yosif Almoshari, Hadil Faris Alotaibi
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引用次数: 0

摘要

摘要:目的:利用高纯度均质技术制备卡铂负载的立方体体。材料与方法:以单油酸甘油酯(GMO)为亲脂载体,以pluronic F-127 (PF-127)和吐温80为添加剂制备了该立方体体。用傅里叶变换红外光谱(FTIR)研究了所有成分的化学相容性,用差示扫描量热法(DSC)进行了热分析,并用x射线衍射(XRD)研究了药物在纯形式和配方中的性质。对制备的立方体体进行了大小、表面电荷、表面形貌、药物释放和药物渗透等方面的表征。结果:FTIR证实了各成分的化学相容性,DSC证实了药物在单独和在立方体中的热稳定性。XRD分析表明,药物为结晶性,但掺入立方体后,结晶度明显降低。制备的长方体为纳米尺寸(直径227 nm),呈立方体状。体外药物释放和渗透研究表明,转基因生物和PF-127的浓度都影响药物的释放和渗透。然而,在3小时的研究中,最大药物释放量为~84%,渗透量为~74%。结论:所选制剂的组成足够适合制备纳米立方体体,具有合适的药物包封效率。
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Formulation and Evaluation of Pluronic F-127 Assisted Carboplatin Cubosomes
Abstract: Objectives: The objective of this study was to prepare carboplatin-loaded cubosomes using high sheer homogenization technique. Materials and Methods: The cubosomes were prepared using Glyceryl Monooleate (GMO) as a lipophilic carrier along with pluronic F-127 (PF-127) and tween 80 as additive of the formulation. All the ingredients were subjected to chemical compatibility studies by Fourier Transform Infra-Red (FTIR) spectroscopy, thermal analysis using Differential Scanning Calorimetry (DSC), whereas X-ray Diffraction (XRD) studies were performed to evaluate the nature of drug in pure form as well as in formulation. The prepared cubosomes were characterized for their size and surface charge, surface morphology, drug release studies and drug permeation studies. Results: FTIR has confirmed the chemical compatibilities of the ingredients, while DSC has exhibited the thermal stabilities of the drug in alone as well as in cubosomes. The XRD has reviled that drug was crystalline, but upon incorporation in cubosmes, the crystallinity has reduced remarkably. The prepared cubosomes were of nanosized (diameter of 227 nm) and cubical in shape. The in vitro drug release and drug permeation studies have showed that concentration of both GMO and PF-127 has effected the release as well as permeation of the drug. However, in 3 hr studies the maximum amount of drug release was ~84% and that of permeation was ~74%. Conclusion: Conclusively, the selected composition of the formulation was suitable enough to prepare the nanosized cubosomes showing suitable entrapment efficiency of the drug.
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
227
审稿时长
>12 weeks
期刊介绍: The official journal of Association of Pharmaceutical Teachers of India (APTI) and is being published since 1967. IJPER, a quarterly publication devoted to publish reviews and research articles in pharmacy and the related disciplines of Pharmaceutical education. It mainly covers the articles of special interest, covering the areas of Pharmaceutical research, teaching and learning, laboratory innovations, education technology, curriculum design, examination reforms, training and other related issues. It encourages debates and discussions on the issues of vital importance to Pharmaceutical education and research. The goal of the journal is to provide the quality publications and publish most important research and review articles in the field of drug development and pharmaceutical education. It is circulated and referred by more than 6000 teachers, 40,000 students and over 1000 professionals working in Pharmaceutical industries, Regulatory departments, hospitals etc.
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