Exploiting the potential of <i>in situ</i> forming liquid crystals: development and <i>in vitro</i> performance of long-acting depots for peptide drug thymosin alpha 1 subcutaneous administration

The fast-growing filed of long-acting depots for subcutaneous (SC) administration holds significant potential to enhance patient adherence to treatment regimens, particularly in the context of chronic diseases. Among them, injectable <i>in situ</i> forming lyotropic liquid crystals (LCCs) consisting of hexagonal mesophases represent an attractive platform due to their remarkable highly ordered microstructure enabling the sustained drug release. These systems are especially relevant for peptide drugs, as their use is limited by their short plasma half-life and inherent poor stability. In this study, we thus aimed to exploit the potential of a liquid crystalline platform for the sustained release of peptide drug thymosin alpha 1 (Tα1), characterized by a short plasma half-life and with that associated twice-weekly SC administration regimen. We initially selected specified ingredients, with ethanol serving to reduce viscosity and stabilize the peptide drug Tα1, lecithin contributing to LCCs formation and stabilization, and glycerol monooleate or glycerol monolinoleate representing the hexagonal LCCs forming matrix material. The selected studied nonaqueous precursor formulations were characterized by suitable rheological properties for SC injection. A convenient and rapid <i>in situ</i> phase transition of precursor formulations to hexagonal LCCs, triggered by water absorption, was successfully accomplished <i>in vitro.</i> Notably, <i>in situ</i> formed LCCs demonstrated sustained release kinetics of the peptide drug Tα1 for up to 2 weeks of <i>in vitro</i> release testing, offering minimized dosing frequency and thus promoting patient adherence. In summary, the newly developed <i>in situ</i> forming liquid crystalline systems represent prospective injectable long-acting depots for SC administration of the peptide drug Tα1.

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Publication Details

Journal
Drug Delivery
Published
2025-03-11
DOI
https://doi.org/10.1080/10717544.2025.2460708
Citations
3
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
4.08
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article

Exploiting the potential of in situ forming liquid crystals: development and in vitro performance of long-acting depots for peptide drug thymosin alpha 1 subcutaneous administration

Robert Roškar, Alenka Zvonar Pobirk, Mercedes Vitek, Mirjam Gosenca Matjaž
3 citations
Drug Delivery
Monoclonal and Polyclonal Antibodies Research
4.08
article

Exploiting the potential of in situ forming liquid crystals: development and in vitro performance of long-acting depots for peptide drug thymosin alpha 1 subcutaneous administration

Robert Roškar, Alenka Zvonar Pobirk, Mercedes Vitek, Mirjam Gosenca Matjaž
article en
3 citations

Abstract

The fast-growing filed of long-acting depots for subcutaneous (SC) administration holds significant potential to enhance patient adherence to treatment regimens, particularly in the context of chronic diseases. Among them, injectable <i>in situ</i> forming lyotropic liquid crystals (LCCs) consisting of hexagonal mesophases represent an attractive platform due to their remarkable highly ordered microstructure enabling the sustained drug release. These systems are especially relevant for peptide drugs, as their use is limited by their short plasma half-life and inherent poor stability. In this study, we thus aimed to exploit the potential of a liquid crystalline platform for the sustained release of peptide drug thymosin alpha 1 (Tα1), characterized by a short plasma half-life and with that associated twice-weekly SC administration regimen. We initially selected specified ingredients, with ethanol serving to reduce viscosity and stabilize the peptide drug Tα1, lecithin contributing to LCCs formation and stabilization, and glycerol monooleate or glycerol monolinoleate representing the hexagonal LCCs forming matrix material. The selected studied nonaqueous precursor formulations were characterized by suitable rheological properties for SC injection. A convenient and rapid <i>in situ</i> phase transition of precursor formulations to hexagonal LCCs, triggered by water absorption, was successfully accomplished <i>in vitro.</i> Notably, <i>in situ</i> formed LCCs demonstrated sustained release kinetics of the peptide drug Tα1 for up to 2 weeks of <i>in vitro</i> release testing, offering minimized dosing frequency and thus promoting patient adherence. In summary, the newly developed <i>in situ</i> forming liquid crystalline systems represent prospective injectable long-acting depots for SC administration of the peptide drug Tα1.

Drug DeliveryVol. 32(1)
University of Ljubljana (SI)
Openalex Percentile: Top 7%
Monoclonal and Polyclonal Antibodies Research
4.08
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