da Silva Arnóbio Antônio, de Matos Jivaldo Rosário, Formariz Thalita Pedroni, Rossanezi Gustavo, Scarpa Maria Virginia, do Egito Eryvaldo Sócrates Tabosa, de Oliveira Anselmo Gomes
Departamento de Fármacos e Medicamentos, Faculdade de Ciências Farmacêuticas, Unesp, Araraquara, São Paulo, Brazil.
Int J Pharm. 2009 Feb 23;368(1-2):45-55. doi: 10.1016/j.ijpharm.2008.09.054. Epub 2008 Oct 15.
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.
热分析已被广泛用于获取有关药物 - 聚合物相互作用的信息以及药物剂型的处方前研究。在这项工作中,通过喷雾干燥制备了具有不同药物:聚合物比例的含曲安奈德(TR)的聚(d,L - 丙交酯 - 乙交酯)(PLGA)可生物降解微粒。本研究的主要目的是使用差示扫描量热法(DSC)、热重分析法(TG)和微商热重分析法(DTG)、X射线分析(XRD)以及红外光谱法(IR)研究喷雾干燥过程不仅对药物 - 聚合物相互作用的影响,还对微粒稳定性的影响。使用DSC、TG和DTG以及IR对药物 - 聚合物相互作用和处方前研究进行了评估。通过高效液相色谱法(HPLC)对包裹在PLGA微粒中的药物进行定量分析。结果表明,对于所有使用的药物:聚合物比例,载药效率都很高,并且用于制备微粒的多晶型为B型。载药微粒的DSC和TG/DTG曲线与各组分物理混合物的曲线非常相似。因此,建立了药物含量与载药PLGA微粒的结构和热性质之间的相关性。这些数据表明喷雾干燥技术不会影响微粒成分的物理化学稳定性。这些结果与IR分析一致,表明在物理混合物和微粒中,TR与PLGA之间均未发生明显的化学相互作用。X射线分析结果与热分析数据一致,表明在载有TR的微粒中,TR的无定形形式占主导,药物的一小部分结晶相也存在。从处方前研究中,我们发现喷雾干燥方法是获得载有TR的PLGA微粒的有效过程。