Engineered Nanoliposomes to Mitigate Osteolytic Bone Lesions in Breast Cancer

Despite advances in breast cancer therapy, its metastasis, particularly to bone, remains a significant challenge. Chemotherapeutic treatment with doxorubicin (DOX) elevates the circulating levels of TGF-β, potentially exacerbating bone metastasis. Moreover, DOX possesses several limitations, such as cardiotoxicity, rapid clearance, and multidrug resistance. Combinatorial therapy utilizing a (transforming growth factor) TGF-β inhibitor along with DOX could substantially reduce the metastatic burden. Baicalein (BAC), a key flavonoid, inhibits the TGF-β signaling pathway, potentially decreasing the bone metastatic ability of DOX. However, BAC is limited by poor solubility, low bioavailability, and a short half-life. Despite these challenges, a low combination index at a molar weight ratio of 1:4 (DOX:BAC) confirmed the synergistic potential of the combination. To deliver the ratiometric dose of both drugs, a PEGylated liposomal formulation loaded with DOX and BAC was developed using the ethanol injection method and evaluated for its anticancer and antimetastatic potential. The particle size of 132.53 ± 1.42 nm with narrow polydispersity and a ζ potential of -26.83 ± 2.2 mV were obtained for the developed nanoliposomes. The ratiometric combination loaded within the liposomal delivery carrier exhibited maximum synergistic activity in the syngeneic 4T1 BALB/c mice tumor model when administered intravenously through the tail vein. Moreover, the liposomal delivery vehicle showed a higher binding affinity toward hydroxyapatite, demonstrating selective bone accumulation. The results indicated efficient targetability and retention at the tumor site, as confirmed by pharmacokinetic profiling. Furthermore, micro-CT analysis revealed the preservation of bone architecture and minimal skeletal damage in treated groups. There was a 4.5-fold increase in the percent bone volume/total volume after treatment with nanoliposomes. These results highlight the promising therapeutic potential of combinatorial DOX and BAC delivery in the treatment of breast cancer-induced bone metastasis.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-10-22
DOI
https://doi.org/10.1021/acsami.5c13155
Primary Topic
Bone health and treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Engineered Nanoliposomes to Mitigate Osteolytic Bone Lesions in Breast Cancer

Manish K. Chourasia, Amit Kumar Kashyap, Jiaur R. Gayen, Amrendra Tiwari et al.
ACS Applied Materials & Interfaces
Bone health and treatments
article

Engineered Nanoliposomes to Mitigate Osteolytic Bone Lesions in Breast Cancer

Manish K. Chourasia, Amit Kumar Kashyap, Jiaur R. Gayen, Amrendra Tiwari, Madhav Nilakanth Mugale, Divya Chauhan, Pooja Yadav, Pavan Kumar Yadav, Naresh Kothuri, Ranjit Kumar, Sonia Verma, Akhilesh Kumar, Durga Prasad Mishra, Manisha Yadav, Candra Wahyu S
article en

Abstract

Despite advances in breast cancer therapy, its metastasis, particularly to bone, remains a significant challenge. Chemotherapeutic treatment with doxorubicin (DOX) elevates the circulating levels of TGF-β, potentially exacerbating bone metastasis. Moreover, DOX possesses several limitations, such as cardiotoxicity, rapid clearance, and multidrug resistance. Combinatorial therapy utilizing a (transforming growth factor) TGF-β inhibitor along with DOX could substantially reduce the metastatic burden. Baicalein (BAC), a key flavonoid, inhibits the TGF-β signaling pathway, potentially decreasing the bone metastatic ability of DOX. However, BAC is limited by poor solubility, low bioavailability, and a short half-life. Despite these challenges, a low combination index at a molar weight ratio of 1:4 (DOX:BAC) confirmed the synergistic potential of the combination. To deliver the ratiometric dose of both drugs, a PEGylated liposomal formulation loaded with DOX and BAC was developed using the ethanol injection method and evaluated for its anticancer and antimetastatic potential. The particle size of 132.53 ± 1.42 nm with narrow polydispersity and a ζ potential of -26.83 ± 2.2 mV were obtained for the developed nanoliposomes. The ratiometric combination loaded within the liposomal delivery carrier exhibited maximum synergistic activity in the syngeneic 4T1 BALB/c mice tumor model when administered intravenously through the tail vein. Moreover, the liposomal delivery vehicle showed a higher binding affinity toward hydroxyapatite, demonstrating selective bone accumulation. The results indicated efficient targetability and retention at the tumor site, as confirmed by pharmacokinetic profiling. Furthermore, micro-CT analysis revealed the preservation of bone architecture and minimal skeletal damage in treated groups. There was a 4.5-fold increase in the percent bone volume/total volume after treatment with nanoliposomes. These results highlight the promising therapeutic potential of combinatorial DOX and BAC delivery in the treatment of breast cancer-induced bone metastasis.

ACS Applied Materials & InterfacesVol. 17(44)
Central Drug Research Institute (IN), PharmacoGenetics (China) (CN), Stanford University (US), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 60%
Bone health and treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.