Non-Absorbable Oral Gentamicin Sulphate: Biopharmaceutical and Dosage Form Evaluation

D. Nwakile, O. Dozie-Nwakile, E. Okoye, C. Umeyor, E.C. Uronnachi, I. Uchendu, A. Attama, V. Okore
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Abstract

Abstract Gentamicin sulphate is an antibiotic belonging to the aminoglycosides and to class III of the Biopharmaceutical Classification System (BCS). Gentamicin sulphate is highly water soluble, but has very low intestinal permeability. The wide use is because of its broad spectrum of activity. In the current study, the suitability of administering gentamicin sulphate orally for local action against susceptible gastrointestinal tract (GIT) bacteria was investigated. The possibility of the drug escaping into the systemic circulation even in the presence of some permeation enhancers was ascertained. Representatives of potential GIT bacteria pathogens were evaluated for their susceptibility to the drug at concentrations obtainable in the GIT using standard microbiological methods. Dose levels that will inhibit these potential bacteria pathogens were also established, as well as the frequency of their administration. Different batches of oral capsules of 250 mg gentamicin sulphate were formulated and their release profiles ascertained using standard methods. The results showed that the selected representatives of the GIT potential pathogenic bacteria were all susceptible to gentamicin sulphate. The drug at its plausible dosage levels of 14.28 mg/kg (1,000 mg/70 kg), 10.71 mg/kg (750 mg/70 kg) and 7.14 mg/kg (500 mg/70 kg) did not cross the mucosal barrier into the systemic circulation even in the presence of some permeation enhancers. The drug's frequency of administration were found to be on 8-hourly bases. Gentamicin sulphate (250 mg) granules formulated with polyethylene glycol (PEG 4000) as granulating aid were quick drying because the granules were not hygroscopic. The formulated gentamicin sulphate capsule batch released enough concentration of the drug that inhibits the test organism within 2 min of dissolution. The above stated doses are acceptable in the dosage form design; it is possible to formulate non-absorbable oral gentamicin sulphate dosage form for local activity in the GIT using existing conventional solid dosage formulating equipment.
不可吸收的口服硫酸庆大霉素:生物制药和剂型评价
摘要硫酸庆大霉素是一种氨基糖苷类抗生素,属于生物药品分类系统(BCS)第III类。硫酸庆大霉素是高度水溶性的,但具有非常低的肠通透性。其广泛的用途是由于其广泛的活性谱。在本研究中,研究了口服硫酸庆大霉素局部作用于敏感胃肠道(GIT)细菌的适用性。甚至在某些渗透促进剂存在的情况下,也确定了药物进入体循环的可能性。使用标准微生物学方法评估潜在胃肠道细菌病原体在胃肠道可获得浓度下对药物的敏感性。还确定了抑制这些潜在细菌病原体的剂量水平以及给药频率。制备了不同批次的硫酸庆大霉素口服胶囊,并用标准方法测定了其释放谱。结果表明,筛选出的GIT潜在致病菌代表菌均对硫酸庆大霉素敏感。在14.28 mg/kg (1,000 mg/70 kg)、10.71 mg/kg (750 mg/70 kg)和7.14 mg/kg (500 mg/70 kg)的合理剂量水平下,即使存在一些渗透促进剂,也没有穿过粘膜屏障进入体循环。药物的给药频率以8小时为单位。以聚乙二醇(peg4000)为造粒剂配制的硫酸庆大霉素颗粒剂(250 mg)由于颗粒不吸湿而快速干燥。配制的硫酸庆大霉素胶囊批在溶解后2分钟内释放出足够浓度的抑制试验生物体的药物。上述剂量在剂型设计中是可接受的;使用现有的常规固体剂型配制设备,可以配制出在胃肠道中具有局部活性的不可吸收的口服硫酸庆大霉素剂型。
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来源期刊
European Pharmaceutical Journal
European Pharmaceutical Journal Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
0.60
自引率
0.00%
发文量
16
期刊介绍: European Pharmaceutical Journal publishes only original articles not previously published and articles that are not being considered or have not been submitted for publication elsewhere. If parts of the results have been published as conference abstract or elsewhere, it should be stated in references. The ethical standards of the Helsinki-Tokio Declaration should be kept. This should be mentioned in the Methods of manuscript. Reviews are published only on request. Authors, whose submitted research work was performed with the support of a company, should indicate this in Conflict of Interest.
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