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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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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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]</description><identifier>ISSN: 0928-0987</identifier><identifier>ISSN: 1879-0720</identifier><identifier>EISSN: 1879-0720</identifier><identifier>DOI: 10.1016/j.ejps.2024.106945</identifier><identifier>PMID: 39489073</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>European journal of pharmaceutical sciences, 2025-01, Vol.204, p.106945, Article 106945</ispartof><rights>2024 The Author(s)</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c237t-1bbc7c58bcf4790e6fd5871aa79b6a6598ff1c66ac17dde71fe05a5906d9d0e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejps.2024.106945$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39489073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xin, Yu</creatorcontrib><creatorcontrib>Fei, Weidong</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Chen, Yue</creatorcontrib><creatorcontrib>Peng, Yujie</creatorcontrib><creatorcontrib>Sun, Dongli</creatorcontrib><creatorcontrib>Zheng, Xiaoling</creatorcontrib><creatorcontrib>Zhu, Xiaojun</creatorcontrib><creatorcontrib>Zhao, Yunchun</creatorcontrib><creatorcontrib>Zheng, Caihong</creatorcontrib><title>Uterine first-pass effect: Unlocking the potential of vaginally administered ritodrine-loaded thermosensitive gel for uterine drug delivery</title><title>European journal of pharmaceutical sciences</title><addtitle>Eur J Pharm Sci</addtitle><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]</description><subject>Administration, Intravaginal</subject><subject>Animals</subject><subject>Drug Delivery Systems - methods</subject><subject>Drug Liberation</subject><subject>Female</subject><subject>Gels</subject><subject>Mice</subject><subject>Pharmacokinetic studies</subject><subject>Poloxamer - administration & dosage</subject><subject>Poloxamer - chemistry</subject><subject>Pregnancy</subject><subject>Premature Birth - prevention & control</subject><subject>Preterm birth</subject><subject>Ritodrine</subject><subject>Ritodrine - administration & dosage</subject><subject>Ritodrine - pharmacokinetics</subject><subject>Temperature</subject><subject>Thermosensitive gel</subject><subject>Tissue Distribution</subject><subject>Tocolytic Agents - administration & dosage</subject><subject>Tocolytic Agents - pharmacokinetics</subject><subject>Uterine first-pass effect</subject><subject>Uterus - drug effects</subject><issn>0928-0987</issn><issn>1879-0720</issn><issn>1879-0720</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcuOEzEQRS0EYsLAD7BAXrLpYPfDD8QGjYAZaSQ2ZG257XJwcLcb2x0p38BPj6MElqxKqrr3lKouQm8p2VJC2YfDFg5L3rak7WuDyX54hjZUcNkQ3pLnaENkKxoiBb9Br3I-EEKY4OQluulkLyTh3Qb92RVIfgbsfMqlWXTOGJwDUz7i3Ryi-eXnPS4_AS-xwFy8Djg6fNR7P-sQTljbyc8-VwpYnHyJ9oxrQtS2NqoxTTHDnH3xR8B7CNjFhNfrVpvWPbYQ6iydXqMXTocMb671Fu2-fvlxd988fv_2cPf5sTFtx0tDx9FwM4jRuJ5LAszZQXCqNZcj02yQwjlqGNOGcmuBUwdk0IMkzEpLgHS36P2Fu6T4e4Vc1OSzgRD0DHHNqqNtJ0jXM1Gl7UVqUsw5gVNL8pNOJ0WJOoegDuocgjqHoC4hVNO7K38dJ7D_LH-_XgWfLgKoVx49JJWNh9mA9al-Xtno_8d_AtJknOI</recordid><startdate>20250101</startdate><enddate>20250101</enddate><creator>Xin, Yu</creator><creator>Fei, Weidong</creator><creator>Zhang, Meng</creator><creator>Chen, Yue</creator><creator>Peng, Yujie</creator><creator>Sun, Dongli</creator><creator>Zheng, Xiaoling</creator><creator>Zhu, Xiaojun</creator><creator>Zhao, Yunchun</creator><creator>Zheng, Caihong</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20250101</creationdate><title>Uterine first-pass effect: Unlocking the potential of vaginally administered ritodrine-loaded thermosensitive gel for uterine drug delivery</title><author>Xin, Yu ; 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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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