The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
A PEGylation-Free Biomimetic Porphyrin Nanoplatform for Personalized Cancer Theranostics
Abstract
PEGylation (PEG) is the most commonly adopted strategy to prolong nanoparticles' vascular circulation by mitigating the reticuloendothelial system uptake. However, there remain many concerns in regards to its immunogenicity, targeting efficiency, etc., which inspires pursuit of alternate, non-PEGylated systems. We introduced here a PEG-free, porphyrin-based ultrasmall nanostructure mimicking nature lipoproteins, termed PLP, that integrates multiple imaging and therapeutic functionalities, including positron emission tomography (PET) imaging, near-infrared (NIR) fluorescence imaging and photodynamic therapy (PDT). With an engineered lipoprotein-mimicking structure, PLP is highly stable in the blood circulation, resulting in favorable pharmacokinetics and biodistribution without the need of PEG. The prompt tumor intracellular trafficking of PLP allows for rapid nanostructure dissociation upon tumor accumulation to release monomeric porphyrins to efficiently generate fluorescence and photodynamic reactivity, which are highly silenced in intact PLP, thus providing an activatable mechanism for low-background NIR fluorescence imaging and tumor-selective PDT. Its intrinsic copper-64 labeling feature allows for noninvasive PET imaging of PLP delivery and quantitative assessment of drug distribution. Using a clinically relevant glioblastoma multiforme model, we demonstrated that PLP enabled accurate delineation of tumor from surrounding healthy brain at size less than 1 mm, exhibiting the potential for intraoperative fluorescence-guided surgery and tumor-selective PDT. Furthermore, we demonstrated the general applicability of PLP for sensitive and accurate detection of primary and metastatic tumors in other clinically relevant animal models. Therefore, PLP offers a biomimetic theranostic nanoplatform for pretreatment stratification using PET and NIR fluorescence imaging and for further customized cancer management via imaging-guided surgery, PDT, or/and potential chemotherapy.
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Cites
Nanoparticle therapeutics: an emerging treatment modality for cancer
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Nanocrystal Core High-Density Lipoproteins: A Multimodality Contrast Agent Platform
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PEGylated nanomedicines: recent progress and remaining concerns
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Cited by
Li, J., Zhen, X., Lyu, Y., Jiang, Y., Huang, J., & Pu, K. (2018) · ACS Nano · doi:10.1021/acsnano.8b04066 · Cited by 377
Wang, T., Wang, D., Yu, H., Wang, M., Liu, J., Feng, B., Zhou, F., Yin, Q., Zhang, Z., Huang, Y., et al. (2016) · ACS Nano · doi:10.1021/acsnano.5b07706 · Cited by 295
Abd Ellah, N. H., & Abouelmagd, S. A. (2017) · Expert Opinion on Drug Delivery · doi:10.1080/17425247.2016.1213238 · Cited by 164
de Maar, J. S., Sofias, A. M., Porta Siegel, T., Vreeken, R. J., Moonen, C., Bos, C., & Deckers, R. (2020) · Theranostics · doi:10.7150/thno.38625 · Cited by 71
Li, M., Lu, Z., Zhang, J., Chen, L., Tang, X., Jiang, Q., Hu, Q., Li, L., Liu, J., & Huang, W. (2023) · Advanced Materials · doi:10.1002/adma.202209647 · Cited by 56
Metadata
- Authors
- Cui, L., Lin, Q., Jin, C. S., Jiang, W., Huang, H., Ding, L., Muhanna, N., Irish, J. C., Wang, F., Chen, J., & Zheng, G.
- Venue
- ACS Nano
- Publisher
- American Chemical Society (ACS)
- Published
- 2015-04-06
- Volume
- 9
- Issue
- 4
- Pages
- 4484-4495
- ISSN
- 1936-0851 (ISSN-L)
- 1936-086X
- OpenAlex
- W2026822060
- Cited by
- 172
- References
- 5
- FWCI
- 11.64
- Type
- journal article
- Language
- en
- Open access
- closed
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- Cui, L., Lin, Q., Jin, C. S., Jiang, W., Huang, H., Ding, L., Muhanna, N., Irish, J. C., Wang, F., Chen, J., & Zheng, G. (2015). A PEGylation-Free Biomimetic Porphyrin Nanoplatform for Personalized Cancer Theranostics. ACS Nano. https://doi.org/10.1021/acsnano.5b01077
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