# Improving the efficacy and targeting of letrozole for the control of breast cancer: in vitro and in vivo studies

**Authors:** Shahira F. El Menshawe, Seif E. Ahmed, Amr Gamal Fouad, Amira H. Hassan

PMC · DOI: 10.1007/s00210-025-04634-6 · Naunyn-Schmiedeberg's Archives of Pharmacology · 2025-10-13

## TL;DR

This study develops a hydrogel formulation of letrozole to improve its effectiveness and targeting in breast cancer treatment.

## Contribution

A novel hydrogel formulation of letrozole is developed to enhance drug delivery and efficacy in breast cancer.

## Key findings

- The LLI hydrogel improved letrozole sustainability by 61.58% and permeation by 3.55-fold.
- The hydrogel reduced tumor volume by 99.69% in a breast cancer rat model.
- Letrozole concentration in the tumor was 9.36 times higher with the hydrogel compared to oral administration.

## Abstract

Letrozole (LTZ) is one of the most widely used treatments for breast cancer (BC). However, several issues can affect its effectiveness and bioavailability when administered orally, including low solubility and uncontrolled release. The primary aim of this study is to develop a hydrogel containing LTZ-loaded invasomes (LLI). This formulation is designed to enhance LTZ’s sustainability, permeability, targeting, bioavailability, and efficacy as a potential treatment for BC. The optimized LLI formulation was established by evaluating various formulations using the Box-Behnken design, focusing on entrapment efficiency and particle size. The LLI hydrogel was created by combining this optimal formulation with 2% Carbopol and was characterized in vitro for viscosity, release kinetics, and permeation. The anti-cancer effects, targeting ability, and safety of the LLI hydrogel were assessed in vivo using the 7,12-dimethylbenz(a)anthracene-induced breast cancer rat model (DIBC). The selected LLI formulation contained 3% phospholipids, 2% ethanol, and 0.5% cineole. Compared to free LTZ, the LLI hydrogel improved LTZ sustainability and permeation by 61.58% and 3.55-fold, respectively. Additionally, the LLI hydrogel reduced tumor volume by 99.69% compared to the DIBC group. Moreover, the concentration of LTZ accumulated in the tumor was 9.36 times greater in the LLI hydrogel than in the oral LTZ group. The transdermal LLI hydrogel represents a promising and safe treatment option for BC.

## Linked entities

- **Chemicals:** letrozole (PubChem CID 3902), ethanol (PubChem CID 702), cineole (PubChem CID 2758), 7,12-dimethylbenz(a)anthracene (PubChem CID 6001)
- **Diseases:** breast cancer (MONDO:0004989)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** BC (MESH:D001943), cancer (MESH:D009369)
- **Chemicals:** ethanol (MESH:D000431), LLI hydrogel (-), 7,12-dimethylbenz(a)anthracene (MESH:D015127), phospholipids (MESH:D010743), Carbopol (MESH:C006912), cineole (MESH:D000077591), LTZ (MESH:D000077289)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935737/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935737/full.md

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Source: https://tomesphere.com/paper/PMC12935737