Uterine first-pass effect: Unlocking the potential of vaginally administered ritodrine-loaded thermosensitive gel for uterine drug delivery

Preterm birth (PTB) remains a leading cause of infant mortality and morbidity, significantly affecting the long-term health, welfare, and development of newborns. Tocolytics, such as ritodrine, a β2-adrenergic receptor agonist, are widely used in developing countries due to their affordability for p...

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Veröffentlicht in:European journal of pharmaceutical sciences 2025-01, Vol.204, p.106945, Article 106945
Hauptverfasser: Xin, Yu, Fei, Weidong, Zhang, Meng, Chen, Yue, Peng, Yujie, Sun, Dongli, Zheng, Xiaoling, Zhu, Xiaojun, Zhao, Yunchun, Zheng, Caihong
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container_issue
container_start_page 106945
container_title European journal of pharmaceutical sciences
container_volume 204
creator Xin, Yu
Fei, Weidong
Zhang, Meng
Chen, Yue
Peng, Yujie
Sun, Dongli
Zheng, Xiaoling
Zhu, Xiaojun
Zhao, Yunchun
Zheng, Caihong
description Preterm birth (PTB) remains a leading cause of infant mortality and morbidity, significantly affecting the long-term health, welfare, and development of newborns. Tocolytics, such as ritodrine, a β2-adrenergic receptor agonist, are widely used in developing countries due to their affordability for preventing PTB by inhibiting uterine contractions. However, ritodrine's short half-life necessitates frequent administration, and prolonged high-dose usage often leads to serious maternal side effects, prompting discontinuation. The uterine first-pass effect, where vaginally administered drugs preferentially target the uterus, can enhance drug concentration in uterine tissue while minimizing systemic absorption and side effects. This study designed a kind of ritodrine-loaded thermosensitive gel (Gel@Rit) to intervene in PTB by exploiting the uterine first-pass effect and investigate its underlying mechanisms. The gel, formulated with poloxamer, demonstrated excellent temperature sensitivity and viscosity, ensuring sustained ritodrine release in vitro. Plasma pharmacokinetic and tissue distribution studies in pregnant mice confirmed the uterine first-pass effect, showing significantly higher drug concentrations in the uterus and markedly lower plasma levels following Gel@Rit administration. The distinctive drug-time curve in Gel@Rit-treated mice, along with uterine tissue fluorescence profiles, elucidated four mechanisms of uterine localization: diffusion through reproductive tract cavities, penetration via vaginal and uterine structures, diffusion through systemic circulation, and retrograde transvaginal veno-uterine artery exchange. This study provides valuable insights into vaginal drug delivery research methodologies, advancing therapeutic strategies for uterine-related conditions and benefiting clinical outcomes in PTB prevention. A schematic diagram depicting the preparation procedure of ritodrine-loaded thermosensitive gel and elucidating the underlying mechanisms facilitating uterine drug delivery via the uterine first-pass effect. [Display omitted]
doi_str_mv 10.1016/j.ejps.2024.106945
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Tocolytics, such as ritodrine, a β2-adrenergic receptor agonist, are widely used in developing countries due to their affordability for preventing PTB by inhibiting uterine contractions. However, ritodrine's short half-life necessitates frequent administration, and prolonged high-dose usage often leads to serious maternal side effects, prompting discontinuation. The uterine first-pass effect, where vaginally administered drugs preferentially target the uterus, can enhance drug concentration in uterine tissue while minimizing systemic absorption and side effects. This study designed a kind of ritodrine-loaded thermosensitive gel (Gel@Rit) to intervene in PTB by exploiting the uterine first-pass effect and investigate its underlying mechanisms. The gel, formulated with poloxamer, demonstrated excellent temperature sensitivity and viscosity, ensuring sustained ritodrine release in vitro. Plasma pharmacokinetic and tissue distribution studies in pregnant mice confirmed the uterine first-pass effect, showing significantly higher drug concentrations in the uterus and markedly lower plasma levels following Gel@Rit administration. The distinctive drug-time curve in Gel@Rit-treated mice, along with uterine tissue fluorescence profiles, elucidated four mechanisms of uterine localization: diffusion through reproductive tract cavities, penetration via vaginal and uterine structures, diffusion through systemic circulation, and retrograde transvaginal veno-uterine artery exchange. This study provides valuable insights into vaginal drug delivery research methodologies, advancing therapeutic strategies for uterine-related conditions and benefiting clinical outcomes in PTB prevention. A schematic diagram depicting the preparation procedure of ritodrine-loaded thermosensitive gel and elucidating the underlying mechanisms facilitating uterine drug delivery via the uterine first-pass effect. 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Tocolytics, such as ritodrine, a β2-adrenergic receptor agonist, are widely used in developing countries due to their affordability for preventing PTB by inhibiting uterine contractions. However, ritodrine's short half-life necessitates frequent administration, and prolonged high-dose usage often leads to serious maternal side effects, prompting discontinuation. The uterine first-pass effect, where vaginally administered drugs preferentially target the uterus, can enhance drug concentration in uterine tissue while minimizing systemic absorption and side effects. This study designed a kind of ritodrine-loaded thermosensitive gel (Gel@Rit) to intervene in PTB by exploiting the uterine first-pass effect and investigate its underlying mechanisms. The gel, formulated with poloxamer, demonstrated excellent temperature sensitivity and viscosity, ensuring sustained ritodrine release in vitro. Plasma pharmacokinetic and tissue distribution studies in pregnant mice confirmed the uterine first-pass effect, showing significantly higher drug concentrations in the uterus and markedly lower plasma levels following Gel@Rit administration. The distinctive drug-time curve in Gel@Rit-treated mice, along with uterine tissue fluorescence profiles, elucidated four mechanisms of uterine localization: diffusion through reproductive tract cavities, penetration via vaginal and uterine structures, diffusion through systemic circulation, and retrograde transvaginal veno-uterine artery exchange. This study provides valuable insights into vaginal drug delivery research methodologies, advancing therapeutic strategies for uterine-related conditions and benefiting clinical outcomes in PTB prevention. A schematic diagram depicting the preparation procedure of ritodrine-loaded thermosensitive gel and elucidating the underlying mechanisms facilitating uterine drug delivery via the uterine first-pass effect. 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subjects Administration, Intravaginal
Animals
Drug Delivery Systems - methods
Drug Liberation
Female
Gels
Mice
Pharmacokinetic studies
Poloxamer - administration & dosage
Poloxamer - chemistry
Pregnancy
Premature Birth - prevention & control
Preterm birth
Ritodrine
Ritodrine - administration & dosage
Ritodrine - pharmacokinetics
Temperature
Thermosensitive gel
Tissue Distribution
Tocolytic Agents - administration & dosage
Tocolytic Agents - pharmacokinetics
Uterine first-pass effect
Uterus - drug effects
title Uterine first-pass effect: Unlocking the potential of vaginally administered ritodrine-loaded thermosensitive gel for uterine drug delivery
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