# Engineering ofloxacin bioavailability through spray-dried HPMC and xanthan gum-based solid dispersions: enhanced solubility and therapeutic efficacy

**Authors:** Sadia Pervez Lali, Arooj Fatima, Muhammad Sher, Muhammad A. Hussain, Muhammad T. Haseeb, Muhammad Naeem-ul-Hassan, Fahad M. Alhoshani, Bandar Khaled Sendy, Ibrahim A. Shaaban, Azhar Abbas

PMC · DOI: 10.1039/d5ra06222e · RSC Advances · 2026-01-28

## TL;DR

This study improves the solubility and effectiveness of the antibiotic ofloxacin using spray-dried solid dispersions with HPMC and xanthan gum.

## Contribution

A novel spray-drying method using HPMC and xanthan gum significantly enhances ofloxacin's solubility and bioavailability.

## Key findings

- Spray-dried dispersions achieved 97.88% and 82.34% drug release compared to 59.2% for unprocessed ofloxacin.
- In vivo studies showed higher Cmax and prolonged half-life in rabbits with spray-dried formulations.
- Hydrogen bonding and amorphous transformation were confirmed to improve solubility.

## Abstract

This study explores the enhancement of oral bioavailability, dissolution rate, and solubility of weakly water-soluble fluoroquinolone antibiotic, ofloxacin (OFL), by solid dispersion (SD) formulation prepared using the spray drying technique. Hydrophilic polymers; hydroxypropyl methylcellulose (HPMC) and xanthan gum (XNG) were used as carriers. FT-IR spectroscopy indicated hydrogen bonding between OFL and the polymer's backbone. DSC and PXRD analyses revealed a transformation from the crystalline to the amorphous state. SEM images revealed reduced particle size and changed surface morphology, which are favorable for solubility improvement. The in vitro drug release studies, performed in simulated gastric conditions (pH 6.8) showed a significant improvement in the drug release, 97.88% and 82.34% for HPMC-based (O–H) and XNG-based (O–X) SDs, respectively, as compared to only 59.2% for unprocessed OFL. Further, in vivo, kinetics reported in a validated HPLC-UV method in rabbits showed an impressive Cmax (O–H: 4.33 µg mL−1; O–X: 4.12 µg mL−1; OFL: 1.8 µg mL−1) and  prolonged t1/2 (8 h vs. 5 h). Thus demonstrating a significant enhancement in bioavailability in the rabbit model. The SDs produced with HPMC and XNG represent a promising strategy to improve the solubility and in vivo performance of OFL, which may translate to improved therapeutic efficacy.

Polymeric spray-dried dispersions of ofloxacin enhance solubility and bioavailability for improved therapeutic efficacy.

## Linked entities

- **Chemicals:** ofloxacin (PubChem CID 4583), hydroxypropyl methylcellulose (PubChem CID 57503849)

## Full-text entities

- **Chemicals:** HPMC (MESH:D065347), XNG (MESH:C002563), fluoroquinolone (MESH:D024841), H (MESH:D006859), water (MESH:D014867), O (MESH:D010100), OFL (MESH:D015242), polymer (MESH:D011108)
- **Species:** Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12848879/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12848879/full.md

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Source: https://tomesphere.com/paper/PMC12848879