Vidyadhara Suryadevara, Sasidhar Reddyvallam Lankapalli, Balakrishna Thalamanchi, Vardhan Malapolu Santha
Department of Pharmaceutics, Chebrolu Hanumaiah Institute of Pharmaceutical Sciences, Chowdavaram, Guntur, Andhra Pradesh, India.
Int J Pharm Investig. 2015 Apr-Jun;5(2):101-6. doi: 10.4103/2230-973X.153387.
The present study deals with the formulation of fast dissolving films of Rizatriptan benzoate that is used for the treatment of Migraine. The concept of fast-dissolving drug delivery emerged from the desire to provide patient with more conventional means of taking their medication.
In the present research work, various trials were carried out using film forming agents such as maltodextrin, gum karaya and xanthan gum to prepare an ideal film. Emulsion evaporation method was used for the preparation of films. The prepared films were evaluated for weight uniformity, drug content, film thickness, folding endurance, dispersion test and curling. The in vitro dissolution studies were carried out using simulated salivary fluid (pH 6.8 phosphate buffer).
About 97% of the drug was found to be released from the film within 10 min that is a desirable character for fast absorption. The drug excipient interaction studies carried out by differential scanning calorimetry analysis and Fourier transform infrared studies revealed that there were no major interactions between the drugs and excipients used for the preparation of films.
Fast dissolving films of Rizatriptan benzoate prepared by emulsion evaporation technique were found to be suitable for eliciting better therapeutic effect in the treatment of migraine.
本研究涉及用于治疗偏头痛的苯甲酸利扎曲普坦速溶膜的制剂。速溶药物递送的概念源于为患者提供更常规服药方式的愿望。
在本研究工作中,使用诸如麦芽糊精、刺梧桐树胶和黄原胶等成膜剂进行了各种试验,以制备理想的膜。采用乳液蒸发法制备膜。对制备的膜进行重量均匀性、药物含量、膜厚度、耐折性、分散试验和卷曲度评估。使用模拟唾液(pH 6.8磷酸盐缓冲液)进行体外溶出研究。
发现约97%的药物在10分钟内从膜中释放出来,这是快速吸收的理想特性。通过差示扫描量热分析和傅里叶变换红外研究进行的药物辅料相互作用研究表明,用于制备膜的药物和辅料之间没有主要相互作用。
通过乳液蒸发技术制备的苯甲酸利扎曲普坦速溶膜被发现适用于在偏头痛治疗中产生更好的治疗效果。