Design of GSH-Responsive Curcumin Nanomicelles for Oesophageal Cancer Therapy.
Zhaoming MaXuzhu GaoFaisal RazaHajra ZafarGuanhong HuangYunyun YangFeng ShiDeqiang WangXia HePublished in: Pharmaceutics (2022)
Oesophageal cancer is a malignant tumor with high morbidity and mortality. Surgical treatment, radiotherapy, and chemotherapy are the most common treatment methods for oesophageal cancer. However, traditional chemotherapy drugs have poor targeting performance and cause serious adverse drug reactions. In this study, a GSH-sensitive material, ATRA-SS-HA, was developed and self-assembled with curcumin, a natural polyphenol antitumor drug, into nanomicelles Cur@ATRA-SS-HA. The micelles had a suitable particle size, excellent drug loading, encapsulation rate, stability, biocompatibility, and stable release behaviour. In the tumor microenvironment, GSH induced disulfide bond rupture in Cur@ATRA-SS-HA and promoted the release of curcumin, improving tumor targeting. Following GSH-induced release, the curcumin IC50 value was significantly lower than that of free curcumin and better than that of 5-FU. In vivo pharmacokinetic experiments showed that the drug-loaded nanomicelles exhibited better metabolic behaviour than free drugs, which greatly increased the blood concentration of curcumin and increased the half-life of the drug. The design of the nanomicelle provides a novel clinical treatment for oesophageal cancer.
Keyphrases
- cancer therapy
- adverse drug
- drug induced
- papillary thyroid
- drug delivery
- squamous cell
- fluorescent probe
- locally advanced
- high glucose
- early stage
- diabetic rats
- squamous cell carcinoma
- emergency department
- lymph node metastasis
- oxidative stress
- radiation therapy
- young adults
- electronic health record
- childhood cancer
- drug release
- hyaluronic acid
- stress induced