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Startseite » News » A combination formulation of TPGS micelles loaded with paclitaxel and olaparib and a pH-thermosensitive hydrogel for treating peritoneal metastasis and drug-resistant ovarian cancer

A combination formulation of TPGS micelles loaded with paclitaxel and olaparib and a pH-thermosensitive hydrogel for treating peritoneal metastasis and drug-resistant ovarian cancer

13. January 2025
A combination formulation of TPGS micelles loaded with paclitaxel and olaparib and a pH-thermosensitive hydrogel for treating peritoneal metastasis and drug-resistant ovarian cancer

A combination formulation of TPGS micelles loaded with paclitaxel and olaparib and a pH-thermosensitive hydrogel for treating peritoneal metastasis and drug-resistant ovarian cancer

Abstract

Purpose

Ovarian cancer (OC) is difficult to detect early; therefore, it is highly likely to advance to peritoneal metastasis at the time of diagnosis. Moreover, multi-drug resistance (MDR) results in a high recurrence rate. To address these issues, the present study aimed to design an intraperitoneally administered formulation combining a d-α-tocopherol polyethylene glycol 1000 succinate (TPGS) micelles loaded with paclitaxel (PTX) and olaparib (OLA) and a pH-thermosensitive hydrogel.

Methods

To assess PTX and OLA’s synergistic effects, we evaluated the combination index (CI) at various molar ratios and physicochemical properties of the formulations and carried out both in vitro and in vivo experiments.

Results

PTX and OLA showed a synergistic effect at all ratios, and considering the various physicochemical properties, a 1:4 ratio using 50 mg of TPGS and a gel polymer concentration of 12.5% w/v was identified as the optimum formulation. In vitro cytotoxicity and cellular uptake assays demonstrated high cytotoxicity of the TPGS micelles compared to those of the free drug and methoxy-poly(ethylene glycol)-poly(ε-caprolactone) (mPEG-PCL) micelles (control) in all formulation groups; TPGS micelles also increased cellular uptake efficiency. Drug release profiles in vitro demonstrated that both PTX and OLA had a release pattern influenced by pH levels, with the slowest release observed at pH 7.4. In vitro and in vivo drug release profiles showed similar release patterns, with PTX showing slower release than OLA.

Conclusion

The final formulation of this study represents a promising therapeutic strategy for OC; however, due to potential toxicity issues of the polymer, its clinical application needs to be further studied.

Read more here

Jo, M.J., Yoon, M.S., Kim, S.Y. et al. A combination formulation of TPGS micelles loaded with paclitaxel and olaparib and a pH-thermosensitive hydrogel for treating peritoneal metastasis and drug-resistant ovarian cancer. J. Pharm. Investig. (2025). https://doi.org/10.1007/s40005-024-00705-7


See also the interesting video on Vitamin E TPGS:

https://www.pharmaexcipients.com/wp-content/uploads/2020/10/vitamin-e-tpgs_ISODEL.mp4

 

Read more here on Vitamin E TPGS 

Tags: excipientsformulation

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