Impact of gastrointestinal differences in veterinary species on the oral drug solubility, in vivo dissolution, and formulation of veterinary therapeutics

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2022-01-01 DOI:10.5599/admet.1140
Marilyn N. Martinez, M. Papich, R. Fahmy
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引用次数: 1

Abstract

Many gaps exist in our understanding of species differences in gastrointestinal (GI) fluid composition and the associated impact of food intake and dietary composition on in vivo drug solubilization. This information gap can lead to uncertainties with regard to how best to formulate pharmaceuticals for veterinary use or the in vitro test conditions that will be most predictive of species-specific in vivo oral product performance. To address these challenges, this overview explores species-specific factors that can influence oral drug solubility and the formulation approaches that can be employed to overcome solubility-associated bioavailability difficulties. These discussions are framed around some of the basic principles associated with drug solubilization, reported species differences in GI fluid composition, types of oral dosage forms typically given for the various animal species, and the effect of prandial state in dogs and cats. This basic information is integrated into a question-and-answer section that addresses some of the formulation issues that can arise in the development of veterinary medicinals.
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兽药物种胃肠道差异对口服药物溶解度、体内溶出度和兽药制剂的影响
我们对不同物种胃肠道(GI)液体组成的差异以及食物摄入和膳食组成对体内药物溶解的相关影响的理解存在许多空白。这种信息差距可能导致在如何最好地配制兽药或最能预测物种特异性体内口服产品性能的体外试验条件方面存在不确定性。为了应对这些挑战,本综述探讨了可能影响口服药物溶解度的物种特异性因素,以及可用于克服溶解度相关生物利用度困难的配方方法。这些讨论围绕着一些与药物增溶有关的基本原则,胃肠道液体组成的物种差异,各种动物通常给予的口服剂型类型,以及狗和猫的膳食状态的影响。这些基本信息被整合到一个问答部分,该部分解决了兽药开发中可能出现的一些配方问题。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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