Pharmacological and biopharmaceutical studies of paracetamol and N-acetyl-D-glucosamine combination as an analgetic drug

Q3 Pharmacology, Toxicology and Pharmaceutics
O. Ruban, I. Zupanets, T. Kolisnyk, S. Shebeko, O. Vashchenko, S. Zimin, O. Dolzhykova
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引用次数: 0

Abstract

The aim. Experimental selection of paracetamol and N-acetyl-D-glucosamine (NAG) ratio and combined dose and bioavailability study of the pharmaceutical composition and active pharmaceutical ingredient (API) in the model of cell biomembranes. Materials and methods. The following substances were used: paracetamol, Actimask Acetaminophen (gelatin-coated paracetamol), and NAG. For pharmacological studies were used laboratory rats, which received test objects intragastrically. The study was performed on the model of inflammatory hyperalgesia according to the Randall-Selitto method. The values of pain threshold before and after pathology induction were established. For biopharmaceutical studies, dry L-α-dimyristoylphosphatidylcholine purchased from Avanti Polar Lipids (purity 99.9 %) was used, hydrated with an appropriate amount of double-distilled water to obtain 70 % wt./wt. water dispersion. Differential scanning calorimetry (DSC) studies were performed employing DSC 1 microcalorimeter (Mettler Toledo). Pharmaceuticals investigated were placed on the bottom of a crucible, then a proper amount of the lipid membrane was added and this moment was taken as the time reference point (t=0). Then a crucible was sealed with a lid and a sample was undergone consecutive temperature scans, heating from 0 to 35 ºC at a scanning rate of 2 ºC/min. The procedure was repeated until no more changes in DSC profiles were observed, i.e. system equilibrium was reached. Results. It has been experimentally proven that the combination of paracetamol and NAG in the ratio of 4:1 showed better analgesic efficacy. The dose of active ingredients was determined to be 50 mg/kg by the sum of API. The active interaction of paracetamol with the bilayer of biomembranes was established and it was determined that Actimask has a worse rate of penetration into the membrane due to the coating of paracetamol with a gelatin shell. NAG didn't significantly affect the rate of penetration of Actimask through the bilayer of membranes, but the auxiliary components of the tablet mixture significantly improved the rate and completeness of penetration of paracetamol through the bilayer of biomembranes. Conclusions. The study found the most effective ratio between paracetamol and NAG in the composition, which is 4:1. The next step was to determine the dose of API, which is 50 mg/kg of the sum of active substances. It has been determined that paracetamol has good permeability through the bilayer of biomembranes, and the tablet mass significantly improves the permeability of paracetamol
对乙酰氨基酚与n -乙酰- d -氨基葡萄糖联用作为镇痛药物的药理学和生物制药研究
的目标。实验选择对乙酰氨基酚与n -乙酰- d -氨基葡萄糖(NAG)的比例、联合剂量及生物利用度研究其药物组成和活性药物成分(API)在细胞生物膜模型中的应用。材料和方法。使用的物质有:扑热息痛、乙酰氨基酚(明胶包被扑热息痛)和NAG。药理学研究用实验室大鼠灌胃接受实验对象。采用Randall-Selitto法对炎症性痛觉过敏模型进行研究。建立病理诱导前后的痛阈值。在生物制药研究中,使用从Avanti Polar Lipids购买的干燥L-α-二myristoyl磷脂酰胆碱(纯度99.9%),用适量的双蒸馏水水化,得到70% wt /wt。水分散。差示扫描量热法(DSC)研究采用DSC - 1微量热计(梅特勒-托莱多)。将所研究的药物置于坩埚底部,然后加入适量的脂质膜,并以此时刻作为时间参考点(t=0)。然后用盖子密封坩埚,对样品进行连续温度扫描,以2ºC/min的扫描速度从0ºC加热到35ºC。重复该过程,直到DSC曲线不再发生变化,即达到系统平衡。结果。实验证明,扑热息痛与NAG以4:1的比例联合使用具有较好的镇痛效果。经原料药之和确定有效成分剂量为50 mg/kg。建立了扑热息痛与生物膜双分子层的活性相互作用,并确定了由于扑热息痛的明胶外壳涂层,Actimask对生物膜的渗透率较差。NAG对乙酰氨基酚双分子膜的渗透速率无显著影响,而片剂混合物的辅助成分显著提高了扑热息痛双分子膜的渗透速率和完整性。结论。研究发现,对乙酰氨基酚和NAG的有效比例为4:1。下一步是测定原料药的剂量,原料药的剂量为活性物质总和的50 mg/kg。经测定,扑热息痛通过生物膜双层具有良好的渗透性,且片剂质量显著提高扑热息痛的渗透性
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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