Folic Acid-Targeted Mixed Pluronic Micelles for Delivery of Triptolide DOI Open Access
Meizhen Yin, Xinying Zhang,

T.Y. Zhang

и другие.

Polymers, Год журнала: 2024, Номер 16(24), С. 3485 - 3485

Опубликована: Дек. 13, 2024

The present study aimed to explore an ideal delivery system for triptolide (TPL) by utilizing the thin-film hydration method prepare drug-loaded, folate-modified mixed pluronic micelles (FA–F-127/F-68–TPL). Scanning electron microscopy and atomic force showed that drug-loaded had a spherical shape with small particle size, average of 30.7 nm. Cell viability experiments FA–F-127/F-68–TPL significantly reduced HepG2 cell viability, exhibiting strong cytotoxicity. Its cytotoxicity was markedly enhanced compared bare TPL. Nile red (Nr) used as model drug FA–F-127/F-68–Nr further validate its tumor-targeting cellular uptake capability. After coincubation cells, multifunctional microplate reader intracellular fluorescence intensity increased, indicating could more effectively enter cells. A nude mouse subcutaneous hepatocellular carcinoma constructed. Following tail vein injection FA–F-127/F-68–Nr, imaging FA–F127/F-68–Nr target tumor tissue, even if entering small-sized challenging, it be excreted through urine. Nude mice were treated injections (45 µg/kg) every other day 21 days. results growth transplanted tumors slowed, no significant difference In summary, exhibits advantages low cost, excellent biological properties, active/passive targeting capabilities, notable against liver cancer inhibition growth. Significantly, FA–F-127/F-68–TPL, despite challenges in insignificant EPR effect, can efficiently via kidneys, thereby preventing release during prolonged circulation potential damage normal tissues. Therefore, represents promising antitumor system.

Язык: Английский

Engineering a pH‐responsive polymeric micelle co‐loaded with paclitaxel and triptolide for breast cancer therapy DOI Creative Commons
Mengmeng Zhang,

Na Ying,

Jie Chen

и другие.

Cell Proliferation, Год журнала: 2024, Номер 57(6)

Опубликована: Янв. 16, 2024

Abstract Breast cancer has overtaken lung as the number one worldwide. Paclitaxel (PTX) is a widely used first‐line anti‐cancer drug, but it not very effective in clinical breast therapy. It been reported that triptolide (TPL) can enhance anticancer effect of paclitaxel, and better synergistic therapeutic effects are seen with concomitant administration PTX TPL. In this study, we developed pH‐responsive polymeric micelles for co‐delivery TPL, which disassembling acidic tumour microenvironments to target drug release effectively kill cells. Firstly, synthesized amphiphilic copolymer mPEG 2000 ‐PBAE through Michael addition reaction, confirmed by various characterizations. Polymer loaded TPL (TPL/PTX‐PMs) were prepared thin film dispersion method. The average particle size TPL/PTX‐PMs was 97.29 ± 1.63 nm, PDI 0.237 0.003 Zeta potential 9.57 0.80 mV, LC% 6.19 0.21%, EE% 88.67 3.06%. Carrier material biocompatibility micelle cytotoxicity assessed using CCK‐8 method, demonstrating excellent biocompatibility. Under same concentration, most toxic cells had strongest proliferation inhibitory effect. Cellular uptake assays revealed significantly increased intracellular concentration enhanced antitumor activity. Overall, micellar promising approach

Язык: Английский

Процитировано

9

Triptolide's Impact on ACER1 Signaling: Inducing Autophagy for Triple-Negative Breast Cancer Suppression DOI

Lingyue Huang,

Rui Xue,

Mingfei Zhu

и другие.

Pathology - Research and Practice, Год журнала: 2025, Номер unknown, С. 155823 - 155823

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

pH-responsive carbohydrate polymer-based nanoparticles in cancer therapy DOI

Nanxi Zhao,

Yang Shi,

Pai Liu

и другие.

International Journal of Biological Macromolecules, Год журнала: 2025, Номер unknown, С. 141236 - 141236

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

A drug-eluting balloon catheter coated with chitosan and paclitaxel-loaded poloxamer-stabilized PLA microparticles for the effective treatment of cholangiocarcinoma DOI

Jin Sil Lee,

Jaehee Jang,

Hyeryeon Oh

и другие.

Journal of Industrial and Engineering Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

αvβ3 integrin aptamer functionalized pH-responsive lipid polymer hybrid nanoparticles for targeted co-delivery of paclitaxel and tamoxifen DOI
Mahavir Narwade, Niladri Haldar,

Rajkumar Samanta

и другие.

International Journal of Biological Macromolecules, Год журнала: 2025, Номер 306, С. 141754 - 141754

Опубликована: Март 4, 2025

Язык: Английский

Процитировано

0

A self-targeting MOFs nanoplatform for treating metastatic triple-negative breast cancer through tumor microenvironment remodeling and chemotherapy potentiation DOI
Hao Wu,

Ming Jin,

Yanhong Liu

и другие.

International Journal of Pharmaceutics, Год журнала: 2024, Номер 664, С. 124625 - 124625

Опубликована: Авг. 30, 2024

Язык: Английский

Процитировано

2

Advances of Stimuli-Responsive Amphiphilic Copolymer Micelles in Tumor Therapy DOI Creative Commons
Yao Wang,

Meng Lin,

Tianfei Fan

и другие.

International Journal of Nanomedicine, Год журнала: 2024, Номер Volume 20, С. 1 - 24

Опубликована: Дек. 31, 2024

Abstract: Amphiphilic copolymers are composed of both hydrophilic and hydrophobic chains, which can self-assemble into polymeric micelles in aqueous solution via the hydrophilic/hydrophobic interactions. Due to their unique properties, have been widely used as drug carriers. Poorly soluble drugs be covalently attached polymer chains or non-covalently incorporated micelles, with improved pharmacokinetic profiles enhanced efficacy. In recent years, stimuli-responsive amphiphilic copolymer attracted significant attention. These respond specific stimuli, including physical triggers (light, temperature, etc). chemical stimuli (pH, redox, physiological factors (enzymes, ATP, Under these structures properties change, enabling targeted therapy controlled release tumors. strategies offer new avenues approaches enhance tumor efficacy reduce side effects. We will review applications different types therapy, aiming provide valuable guidance for future research directions clinical translation. Keywords: stimuli-responsive, delivery system

Язык: Английский

Процитировано

2

Smart hyaluronated micelles to enhance a gemcitabine prodrug efficacy DOI Creative Commons
Ilaria Andreana, Valeria Bincoletto, Caterina Ricci

и другие.

Journal of Drug Delivery Science and Technology, Год журнала: 2024, Номер 104, С. 106518 - 106518

Опубликована: Дек. 11, 2024

Язык: Английский

Процитировано

1

Folic Acid-Targeted Mixed Pluronic Micelles for Delivery of Triptolide DOI Open Access
Meizhen Yin, Xinying Zhang,

T.Y. Zhang

и другие.

Polymers, Год журнала: 2024, Номер 16(24), С. 3485 - 3485

Опубликована: Дек. 13, 2024

The present study aimed to explore an ideal delivery system for triptolide (TPL) by utilizing the thin-film hydration method prepare drug-loaded, folate-modified mixed pluronic micelles (FA–F-127/F-68–TPL). Scanning electron microscopy and atomic force showed that drug-loaded had a spherical shape with small particle size, average of 30.7 nm. Cell viability experiments FA–F-127/F-68–TPL significantly reduced HepG2 cell viability, exhibiting strong cytotoxicity. Its cytotoxicity was markedly enhanced compared bare TPL. Nile red (Nr) used as model drug FA–F-127/F-68–Nr further validate its tumor-targeting cellular uptake capability. After coincubation cells, multifunctional microplate reader intracellular fluorescence intensity increased, indicating could more effectively enter cells. A nude mouse subcutaneous hepatocellular carcinoma constructed. Following tail vein injection FA–F-127/F-68–Nr, imaging FA–F127/F-68–Nr target tumor tissue, even if entering small-sized challenging, it be excreted through urine. Nude mice were treated injections (45 µg/kg) every other day 21 days. results growth transplanted tumors slowed, no significant difference In summary, exhibits advantages low cost, excellent biological properties, active/passive targeting capabilities, notable against liver cancer inhibition growth. Significantly, FA–F-127/F-68–TPL, despite challenges in insignificant EPR effect, can efficiently via kidneys, thereby preventing release during prolonged circulation potential damage normal tissues. Therefore, represents promising antitumor system.

Язык: Английский

Процитировано

0