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Nanotechnology Based Approaches For Enhancements of Bioavailability of Sustain Release Formulation

机译:基于纳米技术的增强缓释制剂生物利用度的方法

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In recent years drug bioavailability has become a subject of matter not only in drug development, additionally within the early stages of drug discovery. Bioavaibility is the major and important pharmacokinetic property of drug. This property of drug is used to describe the fraction of an administered dose of unchanged drug which can reaches to the systemic circulation. When a drug is administered intravenously, its bioavailability is 100%.and if the drug is administered through other routes like oral, its bioavailability decreases because of the incomplete absorption or first pass metabolism. So there is a need in the enhancement of the bioavaibility of sustained release dosage form.This is a consequence of the finding that the majority of candidate drugs that were unsuccessful in clinical trials did so because of problems with absorption, distribution, metabolism, excretion (ADME) and toxicology. Efforts are being created within the Pharmaceutical industry to improve success rates by taking into account the ADME and toxicology aspects in drug discovery. The efficacy of a drug further depends on the ability of the dosage to deliver the active drug to the site of action and at a rate and amount which is sufficient to show the desired pharmacological response. This property is also known as bioavaibility or biologic avaibility.
机译:近年来,不仅在药物开发中,而且在药物发现的早期阶段,药物生物利用度已成为主题。生物利用度是药物的主要和重要的药代动力学性质。药物的这种特性用于描述未达到剂量的可达到全身循环的药物剂量。静脉内给药时,其生物利​​用度为100%。如果通过其他途径(如口服)给药,则由于不完全吸收或首过代谢,其生物利​​用度降低。因此,有必要提高缓释剂型的生物利用度,这是由于发现大多数在临床试验中未成功的候选药物是由于吸收,分布,代谢,排泄( ADME)和毒理学。通过在药物开发中考虑ADME和毒理学方面,正在努力提高制药行业的成功率。药物的功效进一步取决于剂量以足以显示期望的药理反应的速率和量将活性药物递送至作用部位的能力。此属性也称为生物利用度或生物利用度。

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