4.8 Article

In Situ Nanotransformable Hydrogel for Chemo-Photothermal Therapy of Localized Tumors and Targeted Therapy of Highly Metastatic Tumors

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 47, 页码 55862-55878

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c17054

关键词

hydrogel; nanoparticles; passive targeting; melanoma; metastasis

资金

  1. DBT-IYBA [BT/09/IYBA/2015/14]
  2. MHRD IMPRINT 1 [4291, 00275]
  3. MHRD IMPRINT 2 [4291, 00275]
  4. DST INSPIRE [INSPIRE/04/2015/00037, DST/TDT/AMT/2017/227]
  5. Vasudha Foundation [CRG/2020/005069]
  6. CSIR [09/1001(0044)/2019EMR-1]
  7. UGC [938/(OBC) (CSIR-UGC NET Dec.2016)]

向作者/读者索取更多资源

The study developed a smart nanotransforming hydrogel that transformed in situ into polymeric nanoparticles capable of targeting primary and secondary metastatic tumors. The nanoparticles exhibited pH-responsive drug release and demonstrated efficient inhibition of lung metastases in vivo, compared to chemotherapy.
Metastasis is one of the predisposing factors for cancer-related mortalities worldwide. Patients with advanced cancers (stage IV) receive palliative care with minimal possibility of achieving complete remission. Antibody- based therapeutic modalities are capable of targeting tumors that are confined to a particular location but are ineffective in targeting distant secondary tumors. In the current study, we have developed a smart nanotransforming hydrogel (NTG) that transforms in situ to polymeric nanoparticles ( PA NPs) of 100-150 nm when injected subcutaneously. These nanoparticles targeted the primary and secondary metastatic tumors for up to similar to 5 and similar to 3 days, respectively. The in situ-formed PA NPs also demonstrated a pH-responsive drug release resulting in about similar to 80% release within 100 h at 5.8 pH. When tested in vivo, substantial inhibition of lung metastases was observed compared to chemotherapy, thus demonstrating the efficiency of nanotransforming hydrogels in targeting and inhibiting primary and secondary metastatic tumors.

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