A Lanthanum-Tagged Chemotherapeutic Agent HA-Pt to Track the In Vivo Distribution of Hyaluronic Acid Complexes

Ti Zhang, Qiuhong Yang, W. C. Forrest, S. Cai, D. Aires, M. Forrest
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引用次数: 1

Abstract

Hyaluronic acid drug conjugates can target anti-cancer drugs directly to tumor tissue for loco-regional treatment with enhanced bioavailability, local efficacy and reduced toxicity. In this study, the distribution and pharmacokinetics of hyaluronic acid carrier and a conjugated cisplatin anti-cancer drug were tracked by lanthanum (III) [La(III)] affinity tagging of the nanocarrier. The strong binding affinity of La(III) to HA enabled the simple preparation of a physiologically stable complex HA-Pt-La and straightforward simultaneous detection of HA-La and Pt in biological matrices using inductively coupled plasma-mass spectrometry (ICP-MS). Consequently, after subcutaneous injection of HA-Pt-La nanoparticles in human head and neck squamous cell carcinoma (HNSCC) tumor-bearing mice, the HA and Pt content were detected and quantified simultaneously in the plasma, primary tumor, liver and spleen.
镧标记的化疗药物HA-Pt追踪透明质酸复合物在体内的分布
透明质酸药物偶联物可以将抗癌药物直接靶向肿瘤组织进行局部区域治疗,提高生物利用度,局部疗效,降低毒性。本研究利用镧(III) [La(III)]对纳米载体进行亲和标记,追踪透明质酸载体和一种偶联顺铂抗癌药物的分布和药代动力学。La(III)与HA的强结合亲和力使得制备生理稳定的HA-Pt-La复合物变得简单,并且可以使用电感耦合等离子体质谱(ICP-MS)在生物基质中直接同时检测HA-La和Pt。因此,在人头颈部鳞状细胞癌(HNSCC)荷瘤小鼠皮下注射HA-Pt- la纳米粒子后,同时检测和定量血浆、原发肿瘤、肝脏和脾脏中HA和Pt的含量。
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