Advanced Polymers Lab, Instituto Potosino de Investigación Científica y Tecnológica (IPICYT), Camino a la Presa 2055, Lomas 4a, 78216, San Luis Potosí, SLP, Mexico.
Diagnostic and Surgical Sciences Department, Faculty of Dentistry, Universidad de Costa Rica, San Jose, Costa Rica.
J Mater Sci Mater Med. 2021 May 7;32(5):56. doi: 10.1007/s10856-021-06529-3.
The local administration of analgesic combinations by means of degradable polymeric drug delivery systems is an alternative for the management of postoperative pain. We formulated a Tramadol-Dexketoprofen combination (TDC) loaded in poly(vinyl alcohol) (PVA) film. Films were prepared by the solvent casting method using three different molecular weights of PVA and crosslinking those films with citric acid, with the objective of controlling the drug release rate, which was evaluated by UV-vis spectrometry. Non-crosslinked PVA films were also evaluated in the experiments. Differential scanning calorimetry (DSC) analysis of samples corroborated the crosslinking of PVA by the citric acid. Blank and loaded PVA films were tested in vitro for its impact on blood coagulation prothrombin time (PT) and partial thromboplastin time (PTT). The swelling capacity was also evaluated. Crosslinked PVA films of higher-molecular weight showed a prolonged release rate compared with that of the lower-molecular-weight films tested. Non-crosslinked PVA films released 11-14% of TDC. Crosslinked PVA films released 80% of the TDC loaded (p < 0.05). This suggests that crosslinking films can modify the drug release rate. The blank and loaded PVA films induced PT and PTT in the normal range. The results showed that the polymeric films evaluated here have the appropriate properties to allow films to be placed directly on surgical wounds and have the capacity for controlled drug release to promote local analgesia for the control of postoperative pain.
局部给予可生物降解聚合物药物递送系统的镇痛组合是管理术后疼痛的一种替代方法。我们将曲马多-右旋酮洛芬(TDC)组合载入聚乙烯醇(PVA)薄膜中。通过溶剂浇铸法使用三种不同分子量的 PVA 制备薄膜,并使用柠檬酸对其进行交联,目的是控制药物释放速率,通过紫外可见光谱法进行评估。实验中还评估了未交联的 PVA 薄膜。样品的差示扫描量热法(DSC)分析证实了柠檬酸对 PVA 的交联作用。空白和负载 PVA 薄膜在体外测试了对凝血凝血酶原时间(PT)和部分凝血活酶时间(PTT)的影响。还评估了溶胀能力。与测试的低分子量薄膜相比,具有更高分子量的交联 PVA 薄膜显示出更长的释放速率。未交联的 PVA 薄膜释放了 11-14%的 TDC。交联的 PVA 薄膜释放了负载的 TDC 的 80%(p < 0.05)。这表明交联薄膜可以改变药物释放速率。空白和负载的 PVA 薄膜在正常范围内诱导了 PT 和 PTT。结果表明,这里评估的聚合物薄膜具有适当的特性,可直接将薄膜置于手术伤口上,并具有控制药物释放的能力,以促进局部镇痛,控制术后疼痛。