Polymer Coated Nanoparticles for Therapeutic and Diagnostic Applications

A special issue of Nanomaterials (ISSN 2079-4991). This special issue belongs to the section "Biology and Medicines".

Deadline for manuscript submissions: closed (31 March 2022) | Viewed by 5510

Special Issue Editor


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Guest Editor
Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu City, Taiwan
Interests: Polymer chemistry; drug delivery; nanotherapeutic; stimuli-responsive; cancer therapy; nuclear medicine; nanoimmunotherapy

Special Issue Information

Dear Colleagues,

Nanotechnology in medicine offers exciting opportunities in developing nanomaterials for potentiating disease treatment, early diagnostic, prognosis and monitor treatment progression owing to their improved pharmacokinetics and pharmacodynamics of nanotherapeutics.  Selected nanotherapeutics with suitable size, shape, composition, surface charge and functionalization have shown to accumulate in pathological sites while minimizing drugs accumulation elsewhere in the body compared to delivering the drugs without nanoparticle formulation.  A common strategy in designing nanotherapeutic is to encapsulate the drug within the core or conjugated onto the shell of nanoparticles.  In particular, polymer-coated nanoparticles serves as an attractive and modular platform for achieving optimal and tunable nanoparticle size, biocompatibility, surface charge and the ability to deliver toxic cargo and immunotherapy agent upon reaching the disease site.  Since the first FDA approved nanotherapeutic, Doxil, there has been a surge in research publication in developing nanotherapeutic for various disease treatment and diagnostic application.  While nanotherapeutics have shown improved targeting ability, drug solubility, and therapeutic index, and simultaneously reduced systemic toxicity and immunogenicity, the delivery efficiency of nanotherapeutics is sub-optimal.  Over the past 15 years, the nanotherapeutic delivery efficiency has been low with a delivery efficiency hovers ~0.7% in preclinical studies. Low delivery efficiency posed many issues including toxicity in vital organs, increased in the cost of drug and the reduction in treatment efficacy.  To overcome these challenges in delivering nanoparticle therapeutic in vivo, many works has been focused on developing "smart" nanodrug which are responsive to a specific condition within the tumor microenvironment such pH depletion, elevation of tumor-associated enzymes or towards external stimuli such as ultrasound, light, heat and magnetic field has garnered much research interest.  These smart nanodrug are engineered to first exhibit optimal size, surface charge and characteristic for tumor accumulation during blood circulation.  Upon reaching the targeted tumor microenvironment, the nanoparticle will transform into a more cell-interactive manner such as releasing the drug cargo, and enhanced interaction with cell surface upon stimulated with biological or external stimuli. 

In this Special Issues of Polymer Coated Nanoparticles for Therapeutic and Diagnostic Applications, new and novel approaches in the preparation of the stimuli-responsive nanodrug for therapeutic and/or diagnostic application are solicited.    Review articles or research papers exploring various strategy in potentiating anticancer therapy using nanomaterials, multifunctional organic and inorganic nanoparticles as theranostic agent, nanoimmunotherapy and the preparation of nanotherapeutic for combinatorial therapy by releasing orthogonal treatment to the disease site without causing systemic toxicity. 

Prof. Pei Yuin Keng
Guest Editor

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Keywords

  • polymer-coated nanoparticles
  • stimuli-responsive nanoparticles
  • nanotherapeutics
  • nanoimmunotherapy
  • theranostic
  • cancer therapy
  • drug delivery
  • combinatorial therapy
  • molecular imaging
  • nuclear medicine

Published Papers (2 papers)

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Research

18 pages, 3949 KiB  
Article
Polymer-Coated Nanoparticles for Therapeutic and Diagnostic Non-10B Enriched Polymer-Coated Boron Carbon Oxynitride (BCNO) Nanoparticles as Potent BNCT Drug
by Chen-Wei Chiang, Yun-Chen Chien, Wen-Jui Yu, Chia-Yu Ho, Chih-Yi Wang, Tzu-Wei Wang, Chi-Shiun Chiang and Pei-Yuin Keng
Nanomaterials 2021, 11(11), 2936; https://doi.org/10.3390/nano11112936 - 2 Nov 2021
Cited by 12 | Viewed by 3064
Abstract
Boron neutron capture therapy (BNCT) is a powerful and selective anti-cancer therapy utilizing 10B-enriched boron drugs. However, clinical advancement of BCNT is hampered by the insufficient loading of B-10 drugs throughout the solid tumor. Furthermore, the preparation of boron drugs for BNCT [...] Read more.
Boron neutron capture therapy (BNCT) is a powerful and selective anti-cancer therapy utilizing 10B-enriched boron drugs. However, clinical advancement of BCNT is hampered by the insufficient loading of B-10 drugs throughout the solid tumor. Furthermore, the preparation of boron drugs for BNCT relies on the use of the costly B-10 enriched precursor. To overcome these challenges, polymer-coated boron carbon oxynitride (BCNO) nanoparticles, with ~30% of boron, were developed with enhanced biocompatibility, cell uptake, and tumoricidal effect via BNCT. Using the ALTS1C1 cancer cell line, the IC50 of the PEG@BCNO, bare, PEI@BCNO were determined to be 0.3 mg/mL, 0.1 mg/mL, and 0.05 mg/mL, respectively. As a proof-of-concept, the engineered non-10B enriched polymer-coated BCNO exhibited excellent anti-tumor effect via BNCT due to their high boron content per nanoparticle and due to the enhanced cellular internalization and retention compared to small molecular 10B-BPA drug. The astrocytoma ALTS1C1 cells treated with bare, polyethyleneimine-, and polyethylene glycol-coated BCNO exhibited an acute cell death of 24, 37, and 43%, respectively, upon 30 min of neutron irradiation compared to the negligible cell death in PBS-treated and non-irradiated cells. The radical approach proposed in this study addresses the expensive and complex issues of B-10 isotope enrichment process; thus, enabling the preparation of boron drugs at a significantly lower cost, which will facilitate the development of boron drugs for BNCT. Full article
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19 pages, 26783 KiB  
Article
Carbon Dioxide-Derived Biodegradable and Cationic Polycarbonates as a New siRNA Carrier for Gene Therapy in Pancreatic Cancer
by Xinmeng Zhang, Zheng-Ian Lin, Jingyu Yang, Guan-Lin Liu, Zulu Hu, Haoqiang Huang, Xiang Li, Qiqi Liu, Mingze Ma, Zhourui Xu, Gaixia Xu, Ken-Tye Yong, Wei-Chung Tsai, Tzu-Hsien Tsai, Bao-Tsan Ko, Chih-Kuang Chen and Chengbin Yang
Nanomaterials 2021, 11(9), 2312; https://doi.org/10.3390/nano11092312 - 6 Sep 2021
Cited by 19 | Viewed by 3379
Abstract
Pancreatic cancer is an aggressive malignancy associated with poor prognosis and a high tendency in developing infiltration and metastasis. K-ras mutation is a major genetic disorder in pancreatic cancer patient. RNAi-based therapies can be employed for combating pancreatic cancer by silencing K-ras gene [...] Read more.
Pancreatic cancer is an aggressive malignancy associated with poor prognosis and a high tendency in developing infiltration and metastasis. K-ras mutation is a major genetic disorder in pancreatic cancer patient. RNAi-based therapies can be employed for combating pancreatic cancer by silencing K-ras gene expression. However, the clinical application of RNAi technology is appreciably limited by the lack of a proper siRNA delivery system. To tackle this hurdle, cationic poly (cyclohexene carbonate) s (CPCHCs) using widely sourced CO2 as the monomer are subtly synthesized via ring-opening copolymerization (ROCOP) and thiol-ene functionalization. The developed CPCHCs could effectively encapsulate therapeutic siRNA to form CPCHC/siRNA nanoplexes (NPs). Serving as a siRNA carrier, CPCHC possesses biodegradability, negligible cytotoxicity, and high transfection efficiency. In vitro study shows that CPCHCs are capable of effectively protecting siRNA from being degraded by RNase and promoting a sustained endosomal escape of siRNA. After treatment with CPCHC/siRNA NPs, the K-ras gene expression in both pancreatic cancer cell line (PANC-1 and MiaPaCa-2) are significantly down-regulated. Subsequently, the cell growth and migration are considerably inhibited, and the treated cells are induced into cell apoptotic program. These results demonstrate the promising potential of CPCHC-mediated siRNA therapies in pancreatic cancer treatment. Full article
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