Thermal behavior and stability of biodegradable spray-dried microparticles containing triamcinolone

被引:60
作者
da Silva-Junior, Arnobio Antonio [1 ]
de Matos, Jivaldo Rosario [2 ]
Formariz, Thalita Pedroni [1 ]
Rossanezi, Gustavo [1 ]
Scarpa, Maria Virginia [1 ]
Tabosa do Egito, Eryvaldo Socrates [3 ]
de Oliveira, Anselmo Gomes [1 ]
机构
[1] UNESP, Fac Ciencias Farmaceut, Dept Farmacos & Medicamentos, BR-14801902 Araraquara, SP, Brazil
[2] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, BR-09500900 Sao Paulo, Brazil
[3] Univ Fed Rio Grande do Norte, Ctr Ciencias Saude, Dept Farm, BR-59010180 Natal, RN, Brazil
基金
巴西圣保罗研究基金会;
关键词
Triamcinolone; PLGA microparticles; Spray drying; Thermal analysis; X-ray analysis; Thermal stability; DICLOFENAC SODIUM; DRUG-DELIVERY; PHYSICAL STABILITY; SOLID DISPERSION; PEG; 6000; INTRAVITREAL; MICROSPHERES; SYSTEMS; POLY(D; L-LACTIDE-CO-GLYCOLIDE); FORMULATION;
D O I
10.1016/j.ijpharm.2008.09.054
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Thermal analysis has been widely used for obtaining information about drug-polymer interactions and for pre-formulation studies of pharmaceutical dosage forms. In this work, biodegradable microparticles Of Poly (D,L-lactide-co-glycolide) (PLGA) containing triamcinolone (TR) in various drug:polymer ratios were produced by spray drying. The main purpose of this study was to study the effect of the spray-drying process not only on the drug-polymer interactions but also on the stability of microparticles using differential scanning calorimetry (DSC), thermogravimetry (TG) and derivative thermogravimetry (DTG), X-ray analysis (XRD), and infrared spectroscopy (IR). The evaluation of drug-polymer interactions and the pre-formulation studies were assessed using the DSC, TG and DTG, and IR. The quantitative analysis of drugs entrapped in PLGA microparticles was performed by the HPLC method. The results showed high levels of drug-loading efficiency for all used drug: polymer ratio, and the polymorph used for preparing the microparticles was the form B. The DSC and TG/DTG profiles for drug-loaded microparticles were very similar to those for the physical mixtures of the components. Therefore, a correlation between drug content and the structural and thermal properties of drug-loaded PLGA microparticles was established. These data indicate that the spray-drying technique does not affect the physico-chemical stability of the microparticle components. These results are in agreement with the IR analysis demonstrating that no significant chemical interaction occurs between TR and PLGA in both physical mixtures and microparticles. The results of the X-ray analysis are in agreement with the thermal analysis data showing that the amorphous form of TR prevails over a small fraction of crystalline phase of the drug also present in the TR-loaded microparticles. From the pre-formulation studies, we have found that the spray-drying methodology is an efficient process for obtaining TR-loaded PLGA microparticles. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 55
页数:11
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