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Combined Ibuprofen-Nanoconjugate Micelles with E-Selectin for Effective Sunitinib Anticancer Therapy
Xianhu Zeng1, Yi Teng1, Chunrong Zhu2
1Department of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, People's Republic of China.
Introduction:
Sunitinib, a first-line therapy with a certain effect, was utilized in the early stages of renal cell carcinoma treatment. However, its clinical toxicity, side effects, and its limited bioavailability, resulted in inadequate clinical therapeutic efficacy. Building neoteric, simple, and safe drug delivery systems with existing drugs offers new options. Therefore, we aimed to construct a micelle to improve the clinical efficacy of sunitinib by reusing ibuprofen.
Methods:
We synthesized the sialic acid-poly (ethylene glycol)-ibuprofen (SA-PEG-IBU) amphipathic conjugate in two-step reaction. The SA-PEG-IBU amphiphilic conjugates can form into stable SPI nanomicelles in aqueous solution, which can be further loaded sunitinib (SU) to obtain the SPI/SU system. Following nanomicelle creation, sialic acid exposed to the nanomicelle surface can recognize the overexpressed E-selectin receptor on the membrane of cancer cells to enhance cellular uptake. The properties of morphology, stability, and drug release about the SPI/SU nanomicelles were investigated. Confocal microscopy and flow cytometry were used to assess the cellular uptake efficiency of nanomicelles in vitro. Finally, a xenograft tumor model in nude mice was constructed to investigate the body distribution and tumor suppression of SPI/SU in vivo.
Results:
The result showed that SPI nanomicelles exhibited excellent tumor targeting performance and inhibited the migration and invasion of tumor cell in vitro. The SPI nanomicelles can improve the accumulation of drugs in the tumor site that showed effective tumor inhibition in vivo. In addition, H&E staining and immunohistochemical analysis demonstrated that the SPI/SU nanomicelles had a superior therapeutic effect and lower biotoxicity.
Conclusion:
The SPI/SU nanomicelles displayed excellent anti-tumor ability, and can suppress the metastasis of tumor cell by decreasing the expression of Cyclooxygenase-2 due to the ibuprofen, providing an optimistic clinical application potential by developing a simple but safe drug delivery system.
Insights
This study developed novel nanomicelles using ibuprofen and sunitinib to improve renal cell carcinoma treatment. The new system enhances drug delivery, reduces toxicity, and shows promising anti-tumor effects in preclinical models.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Oncology
Background:
- Sunitinib is a first-line renal cell carcinoma (RCC) therapy with limited efficacy due to toxicity and poor bioavailability.
- Developing novel drug delivery systems is crucial for enhancing existing cancer therapies.
Purpose of the Study:
- To create a safe and effective micelle-based drug delivery system for sunitinib using ibuprofen.
- To improve the clinical efficacy and reduce the toxicity of sunitinib in RCC treatment.
Main Methods:
- Synthesized sialic acid-poly(ethylene glycol)-ibuprofen (SA-PEG-IBU) conjugates to form nanomicelles.
- Loaded sunitinib (SU) into SA-PEG-IBU nanomicelles (SPI/SU) for targeted cancer cell delivery.
- Evaluated nanomicelle properties, in vitro cellular uptake, and in vivo anti-tumor efficacy in a xenograft model.
Main Results:
- SPI nanomicelles demonstrated effective tumor targeting and inhibited cancer cell migration and invasion in vitro.
- SPI/SU nanomicelles enhanced drug accumulation at tumor sites, leading to significant tumor inhibition in vivo.
- SPI/SU nanomicelles exhibited superior therapeutic effects with reduced biotoxicity compared to sunitinib alone.
Conclusions:
- SPI/SU nanomicelles show potent anti-tumor activity and can suppress metastasis by downregulating Cyclooxygenase-2.
- This simple and safe drug delivery system holds significant potential for clinical application in cancer therapy.
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