Engineering long-acting injectable in situ forming implants for sustained delivery of citalopram in depression management

Long-acting injectable formulations have emerged as promising systems for managing chronic psychiatric conditions by reducing dosing frequency and improving patient adherence. Oral antidepressants such as citalopram hydrobromide require daily administration, posing a significant risk of non-compliance in patients with Major Depressive Disorder (MDD). This study aimed to develop and characterize a poly (lactic-co-glycolic acid) (PLGA)-based in situ forming implant (ISFI) for the sustained parenteral delivery of citalopram hydrobromide over 10 days. Systematic formulation screening across polymers, solvents, and lipid excipients identified the optimized formulation (F4) composition, which was evaluated for viscosity, syringeability, in vitro drug release, ex vivo depot formation, release kinetics, cytotoxicity, and in vivo pharmacokinetic prediction. The optimized formulation exhibited Newtonian flow behavior (viscosity 0.35 Pa.s) with a maximum expulsion force of 16.49 N through a 20G needle, confirming adequate injectability. The in vitro release profile demonstrated a moderate initial burst of ~ 13% within 24 h, followed by near-linear sustained release reaching ~ 87% by Day 10. The Korsmeyer-Peppas model provided the best fit (R² = 0.99, n = 0.865), confirming Super case II and non-Fickian diffusion-erosion transport. A strong in vitro-ex vivo correlation (R² = 0.9259) validated the release model. Cytotoxicity assessment confirmed biocompatibility with an IC₅₀ of 34.92 ± 2.28 µg/mL, representing a 300-fold safety margin above therapeutic plasma concentrations. Convolution-based pharmacokinetic prediction demonstrated sustained systemic exposure over 10 days from a single intramuscular injection. This study demonstrates the feasibility of a PLGA-based long-acting injectable platform for sustained citalopram delivery, supporting its potential utility in the management of Major Depressive Disorder.

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Publication Details

Journal
Drug Delivery and Translational Research
Published
2026-10-14
DOI
https://doi.org/10.1007/s13346-026-02230-6
Primary Topic
Advanced Drug Delivery Systems
Type
article
Field-Weighted Citation Impact
0.00

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article

Engineering long-acting injectable in situ forming implants for sustained delivery of citalopram in depression management

Weranga Rajapaksha, Deepa Nakmode, Sanjay Garg, HariPriya Koppisetti et al.
Drug Delivery and Translational Research
Advanced Drug Delivery Systems
article

Engineering long-acting injectable in situ forming implants for sustained delivery of citalopram in depression management

Weranga Rajapaksha, Deepa Nakmode, Sanjay Garg, HariPriya Koppisetti, Yunmei Song, Souha Youssef, Baljinder Singh
article en

Abstract

Long-acting injectable formulations have emerged as promising systems for managing chronic psychiatric conditions by reducing dosing frequency and improving patient adherence. Oral antidepressants such as citalopram hydrobromide require daily administration, posing a significant risk of non-compliance in patients with Major Depressive Disorder (MDD). This study aimed to develop and characterize a poly (lactic-co-glycolic acid) (PLGA)-based in situ forming implant (ISFI) for the sustained parenteral delivery of citalopram hydrobromide over 10 days. Systematic formulation screening across polymers, solvents, and lipid excipients identified the optimized formulation (F4) composition, which was evaluated for viscosity, syringeability, in vitro drug release, ex vivo depot formation, release kinetics, cytotoxicity, and in vivo pharmacokinetic prediction. The optimized formulation exhibited Newtonian flow behavior (viscosity 0.35 Pa.s) with a maximum expulsion force of 16.49 N through a 20G needle, confirming adequate injectability. The in vitro release profile demonstrated a moderate initial burst of ~ 13% within 24 h, followed by near-linear sustained release reaching ~ 87% by Day 10. The Korsmeyer-Peppas model provided the best fit (R² = 0.99, n = 0.865), confirming Super case II and non-Fickian diffusion-erosion transport. A strong in vitro-ex vivo correlation (R² = 0.9259) validated the release model. Cytotoxicity assessment confirmed biocompatibility with an IC₅₀ of 34.92 ± 2.28 µg/mL, representing a 300-fold safety margin above therapeutic plasma concentrations. Convolution-based pharmacokinetic prediction demonstrated sustained systemic exposure over 10 days from a single intramuscular injection. This study demonstrates the feasibility of a PLGA-based long-acting injectable platform for sustained citalopram delivery, supporting its potential utility in the management of Major Depressive Disorder.

Drug Delivery and Translational Research
The University of Adelaide (AU)
University of South Australia
Good health and well-being
Openalex Percentile: Top 17%
Advanced Drug Delivery Systems
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