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评价基于葫芦脲的三元主体-客体配合物在生理环境中的稳定性及超分子诊疗纳米医学的构建。

Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine.

机构信息

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, People's Republic of China.

Department of Rehabilitation Medicine, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, People's Republic of China.

出版信息

J Nanobiotechnology. 2021 Oct 20;19(1):330. doi: 10.1186/s12951-021-01076-z.

Abstract

BACKGROUND

Supramolecular theranostics have exhibited promising potentials in disease diagnosis and therapy by taking advantages of the dynamic and reversible nature of non-covalent interactions. It is extremely important to figure out the stability of the driving forces in physiological environment for the preparation of theranostic systems.

METHODS

The host-guest complexation between cucurbit[8]uril (CB[8]), 4,4'-bipyridinium, and napththyl guest was fully studied using various characterizations, including nuclear magnetic resonance spectroscopy, ultraviolet-visible (UV-vis) spectroscopy, isothermal titration calorimetry (ITC). The association constants of this ternary complex were determined using isothermal titration calorimetry. The stability of the non-covalent interactions and self-assemblies form from this molecular recognition was confirmed by UV-vis spectroscopy and dynamic light scattering (DLS). A supramolecular nanomedicine was constructed on the basis of this 1:1:1 ternary recognition, and its in vitro and in vivo anticancer efficacy were thoroughly evaluated. Positron emission tomography (PET) imaging was used to monitor the delivery and biodistribution of the supramolecular nanomedicine.

RESULTS

Various experiments confirmed that the ternary complexation between 4,4'-bipyridinium, and napththyl derivative and CB[8] was stable in physiological environment, including phosphate buffered solution and cell culture medium. Supramolecular nanomedicine (SNM@DOX) encapsulating a neutral anticancer drug (doxrubincin, DOX) was prepared based on this molecular recognition that linked the hydrophobic poly(ε-caprolactone) chain and hydrophilic polyethylene glycol segment. The non-covalent interactions guaranteed the stability of SNM@DOX during blood circulation and promoted its tumor accumulation by taking advantage of the enhanced permeability and retention effect, thus greatly improving the anti-tumor efficacy as compared with the free drug.

CONCLUSION

Arising from the host-enhanced charge-transfer interactions, the CB[8]-based ternary recognition was stable enough in physiological environment, which was suitable for the fabrication of supramolecular nanotheranostics showing promising potentials in precise cancer diagnosis and therapy.

摘要

背景

超分子治疗学利用非共价相互作用的动态和可逆性质,在疾病诊断和治疗方面表现出了巨大的潜力。了解生理环境中驱动力的稳定性对于治疗系统的制备非常重要。

方法

通过各种表征,包括核磁共振波谱、紫外-可见(UV-vis)光谱、等温热力学滴定(ITC),充分研究了葫芦[8]脲(CB[8])、4,4'-联吡啶和萘基客体之间的主客体络合作用。使用等温滴定微量热法确定了这种三元络合物的结合常数。通过紫外-可见光谱和动态光散射(DLS)证实了这种分子识别形成的非共价相互作用和自组装的稳定性。在此 1:1:1 三元识别的基础上构建了超分子纳米医学,并对其体外和体内抗癌疗效进行了全面评价。正电子发射断层扫描(PET)成像用于监测超分子纳米药物的递送和生物分布。

结果

各种实验证实,在生理环境中,包括磷酸盐缓冲溶液和细胞培养基中,4,4'-联吡啶和萘基衍生物与 CB[8]之间的三元络合作用是稳定的。基于这种分子识别,制备了超分子纳米药物(SNM@DOX),它封装了一种中性抗癌药物(阿霉素,DOX),连接了疏水性聚(ε-己内酯)链和亲水性聚乙二醇段。非共价相互作用保证了 SNM@DOX 在血液循环中的稳定性,并利用增强的渗透性和保留效应促进其肿瘤积累,从而大大提高了与游离药物相比的抗癌疗效。

结论

基于 CB[8]的三元识别由于主体增强的电荷转移相互作用,在生理环境中足够稳定,适用于制备超分子纳米治疗学,在精确癌症诊断和治疗方面具有巨大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd94/8529793/b86e8402e888/12951_2021_1076_Sch1_HTML.jpg

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