Mirza Mohd Aamir, Ahmad Niyaz, Agarwal Suraj Prakash, Mahmood Danish, Khalid Anwer M, Iqbal Z
Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard, New Delhi 11006, India.
Department of Pharmacology, Faculty of Pharmacy, Jamia Hamdard, New Delhi, India.
Results Pharma Sci. 2011 Jul 12;1(1):16-26. doi: 10.1016/j.rinphs.2011.06.001. eCollection 2011 May.
Major and biologically most explored components of natural organic matter (NOM) are humic acid (HA) and fulvic acid (FA). We have explored rock shilajit as a source of NOM. On the other hand carbamazepine (CBZ) is a well known anticonvulsant drug and has a limited accessibility to brain. Bioavailability and pharmacokinetic profiles of CBZ have been improved by complexation and different techniques also. Present study has assessed the comparative abilities of FA and HA as complexing agent for CBZ in order to enhance pharmacokinetic profile of CBZ and accessibility to the brain. These two complexing agents have been compared on various indices such as their abilities to cause complexation and enhance solubility, permeability and dissolution. The present study also compared pharmacodynamic and biochemical profiles after oral administration of complexes. With the help of various pharmaceutical techniques such as freeze drying, physical mixture, kneading and solvent evaporation, two molar ratios (1:1 and 1:2) were selected for complexation and evaluated for conformational analysis (molecular modeling). Complex formed was further characterized by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), mass spectroscopy and X-ray diffraction (XRD). Preclinical study on rodents with CBZ-HA and CBZ-FA has yielded appreciable results in terms of their anticonvulsant and antioxidants activities. However, CBZ-HA (1:2) demonstrated better result than any other complex.
天然有机物(NOM)的主要成分以及生物学上研究最多的成分是腐殖酸(HA)和富里酸(FA)。我们已探索将岩石希拉季特作为NOM的来源。另一方面,卡马西平(CBZ)是一种著名的抗惊厥药物,其进入大脑的能力有限。通过络合和其他不同技术,卡马西平的生物利用度和药代动力学特征也得到了改善。本研究评估了FA和HA作为CBZ络合剂的相对能力,以增强CBZ的药代动力学特征及其进入大脑的能力。已在各种指标上对这两种络合剂进行了比较,例如它们引起络合以及增强溶解度、渗透性和溶解性的能力。本研究还比较了口服复合物后的药效学和生化特征。借助冷冻干燥、物理混合、捏合和溶剂蒸发等各种制药技术,选择了两个摩尔比(1:1和1:2)进行络合,并对其进行构象分析(分子建模)评估。形成的络合物通过差示扫描量热法(DSC)、傅里叶变换红外光谱(FT-IR)、质谱和X射线衍射(XRD)进一步表征。对使用CBZ-HA和CBZ-FA的啮齿动物进行的临床前研究在其抗惊厥和抗氧化活性方面取得了显著成果。然而,CBZ-HA(1:2)表现出比任何其他络合物都更好的效果。