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首页> 外文期刊>Pharmaceutical research >Pharmacologic and pharmacokinetic assessment of anti-TGFbeta2 aptamers in rabbit plasma and aqueous humor.
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Pharmacologic and pharmacokinetic assessment of anti-TGFbeta2 aptamers in rabbit plasma and aqueous humor.

机译:抗TGFbeta2适体在兔血浆和房水中的药理和药代动力学评估。

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摘要

PURPOSE: The aim of the study is to determine the bioactivity and effects of PEGylation on the pharmacokinetics in rabbit aqueous humor and plasma of an aptamer directed against TGFbeta2. METHODS: Pharmacological activity of anti-TGFbeta2 aptamer in rabbit ocular fluid was demonstrated using a mink lung epithelial cell proliferation assay. For pharmacokinetic analyses, concentrations of aptamers in plasma and aqueous humor were determined over time following bilateral subconjunctival administration to Dutch-belted rabbits using a hybridization-based pseudo-enzyme-linked immunosorbent assay (ELISA) assay. RESULTS: Anti-TGFbeta2 aptamer (ARC81) binds to human TGFbeta2 with a K(D) of approximately 5 nM and inhibits the activity of human TGFbeta2 in vitro in a cell-based assay with an IC(50) of approximately 100 nM. ARC81 blocks endogenously derived TGFbeta2 in rabbit aqueous humor in vitro with an IC(50) of approximately 200 nM and an IC(90) of approximately 1 microM. In vivo in rabbit, ARC81 [no polyethylene glycol (PEG)] entered systemic circulation rapidly (t(max) = 1 h in plasma) relative to aptamer conjugates ARC117 (20 kDa PEG) and ARC119 (40 kDa PEG), which showed prolonged residence in the subconjunctival space and aqueous compartment (t(max) = 6 and 12 h, respectively, in plasma). Both 20- and 40-kDa aptamer conjugates reached maximal concentrations (C(max)) in aqueous humor of 23-30 nM and remained at or above 1 nM for as long as 12 h. CONCLUSIONS: Pharmacologically active levels of anti-TGFbeta2 aptamers can be sustained in the ocular fluid and local tissue environment over a 12-h period after single administration. Daily subconjunctival administration of PEGylated anti-TGFbeta2 aptamers should allow further pharmacological evaluation of these agents in a rabbit conjunctival scarring model. Perioperative administration, via subconjunctival injection, may prove to be an effective means to deliver therapeutic quantities of TGFbeta2 aptamer conjugates in trabeculectomy procedures.
机译:目的:本研究的目的是确定针对兔TGFβ2的适体在兔房水和血浆中的生物活性和聚乙二醇化对药代动力学的影响。方法:采用水貂肺上皮细胞增殖试验证明抗TGFβ2适体在兔眼液中的药理活性。对于药代动力学分析,使用基于杂交的假酶联免疫吸附测定(ELISA)方法,对荷兰带状兔子双眼结膜下给药后,随时间测定血浆和房水中适体的浓度。结果:抗TGFbeta2适体(ARC81)以约5 nM的K(D)结合人TGFbeta2,并在基于细胞的测定中以约100 nM的IC(50)抑制人TGFbeta2的活性。 ARC81阻断兔房水中的内源性衍生TGFbeta2,IC(50)约为200 nM,IC(90)约为1 microM。在体内,相对于适体偶联物ARC117(20 kDa PEG)和ARC119(40 kDa PEG),ARC81 [无聚乙二醇(PEG)]迅速进入系统循环(血浆中t(max)= 1 h)。保留在结膜下空间和水隔室中(在血浆中分别为t(max)= 6和12 h)。 20kDa和40kDa的适体缀合物在房水中均达到23-30 nM的最大浓度(C(max)),并保持在1 nM或以上长达12 h。结论:抗TGFβ2适体的药理活性水平可以在单次给药后12小时内在眼液和局部组织环境中维持。每天进行结膜下聚乙二醇化抗TGFbeta2适体的管理应允许在兔结膜瘢痕形成模型中对这些药物进行进一步的药理评估。通过结膜下注射进行围手术期给药可能被证明是在小梁切除术中递送治疗量的TGFbeta2适体偶联物的有效手段。

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