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In situ chemically crosslinked injectable hydrogels for the subcutaneous delivery of trastuzumab to treat breast cancer

机译:原位化学交联的可注射水凝胶,用于皮下递送曲妥珠单抗治疗乳腺癌

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摘要

Recently, novel approaches for the delivery of therapeutic antibodies have attracted much attention, especially sustained release formulations. However, sustained release formulations capable of carrying a high antibody load remain a challenge for practical use. In this study, a novel injectable hydrogel composed of maleimide-modified gamma-polyglutamic acid (gamma-PGA-MA) and thiol end-functionalized 4-arm poly (ethylene glycol) (4-arm PEG-SH) was developed for the subcutaneous delivery of trastuzumab. gamma-PGA-MA and 4-arm PEG-SH formed a hydrogel through thiol-maleimide reactions, which had shear-thinning properties and reversible rheological behaviors. Moreover, a high content of trastuzumab (100 mg/mL) could be loaded into this hydrogel, and trastuzumab demonstrated a sustained release over several weeks through electrostatic attraction. In addition, trastuzumab released from the hydrogel had adequate stability in terms of its structural integrity, binding bioactivity, and antiproliferative effect on BT-474 cells. Pharmacokinetic studies demonstrated that trastuzumab-loaded hydrogel (Her-hydrogel-10, composed of 1.5% gamma-PGA-MA, 1.5% 4-arm PEG-SH, and 10 mg/mL trastuzumab) and trastuzumab/Zn-loaded hydro-gel (Her/Zn-hydrogel-10, composed of 1.5% gamma-PGA-MA, 1.5% 4-arm PEG-SH, 5 mM ZnCl2, and 10 mg/mL trastuzumab) could lower the maximum plasma concentration (C-max) than the trastuzumab solution. Furthermore, Her/Zn-hydrogel-10 was better able to release trastuzumab in a controlled manner, which was ascribed to electrostatic attraction and formation of trastuzumab/Zn nanocomplexes. In a BT-474 xenograft tumor model, Her-hydrogel-10 had a similar tumor growth-inhibitory effect as that of the trastuzumab solution. By contrast, Her/Zn-hydrogel-10 exhibited a superior tumor growth-inhibitory capability due to the functionality of Zn. This study demonstrated that this hydrogel has potential as a carrier for the local and systemic delivery of proteins and antibodies.
机译:最近,递送治疗性抗体的新方法引起了许多关注,特别是持续的释放制剂。然而,能够携带高抗体负荷的持续释放制剂仍然是实际使用的挑战。在该研究中,为皮下制定了一种由马来酰亚胺改性的γ-聚谷氨酸(γ-PGA-MA)和硫醇端官能化的4臂聚(乙二醇)(4臂PEG-SH)组成的新型可注射水凝胶。交付曲妥珠单抗。 γ-PGA-MA和4臂PEG-SH通过硫醇 - 马来酰亚胺反应形成水凝胶,其具有剪切稀疏性能和可逆的流变行为。此外,可以将高含量的曲妥珠单抗(& 100mg / ml)加载到该水凝胶中,并且Trastuzumab通过静电吸引显示在几周内持续释放。此外,在水凝胶中释放的曲妥珠单抗在其结构完整性,结合生物活性和对BT-474细胞上的抗增殖作用方面具有足够的稳定性。药代动力学研究表明,曲妥珠珠猴加载水凝胶(HER-HYROLOL-10,由1.5%γ-PGA-MA,1.5%4臂PEG-SH和10mg / mL曲妥珠单抗组成)和曲妥珠单抗/ Zn负载水凝胶(由γ-pga-mA,1.5%4臂PEG-SH,5mM ZnCl2和10mg / ml曲据的10mM ZnCl2和10mg / ml曲妥珠单抗组成,可以降低最大血浆浓度(C-MAX)组成的(HER / Zn-Hydrogel-10。比曲妥珠单抗解决方案。此外,HER / Zn-HydroLogel-10更好地能够以受控方式释放曲妥珠单抗,其归因于静电吸引和形成曲妥珠单抗/ Zn纳米复合物。在BT-474异种移植肿瘤模型中,Her-HydroLogel-10具有与曲妥珠单抗溶液的肿瘤生长抑制效果类似。相比之下,由于Zn的功能,HER / Zn-Hydrogel-10表现出优异的肿瘤生长抑制能力。该研究表明,该水凝胶具有局部和全身递送蛋白质和抗体的载体。

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