• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于药物离子对和低聚离子液体构建伊马替尼控释成膜系统用于皮肤黑色素瘤的长效局部治疗

Construction of Imatinib Controlled Release Film-Forming System Based on Drug Ion-Pair and Oligomeric Ionic Liquids for the Long Local Therapy of Cutaneous Melanoma.

作者信息

Wang Junzhu, Sun Han, Jia Wenxuan, Song Yilin, Quan Peng, Fang Liang, Liu Chao

机构信息

Department of Pharmaceutical Sciences, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, 110016, Liaoning, China.

出版信息

AAPS PharmSciTech. 2023 Mar 25;24(4):87. doi: 10.1208/s12249-023-02546-3.

DOI:10.1208/s12249-023-02546-3
PMID:36964446
Abstract

An imatinib controlled release film-forming system (FFS) was developed based on the drug ion-pair and newly designed oligomeric ionic liquids (OILs) for the topical therapy of cutaneous melanoma, which avoided the systemic side-effect of oral administration and maintained a long local therapy effect. The OILs significantly improved the drug release capacity about 1.5-fold, and the formability and stability of FFSs (verified by AFM/PLM). The in vivo anti-tumor efficacy studies in melanoma tumor bearing mice showed that compared with the oral capsules, the topical application of the optimized imatinib FFS significantly (p < 0.01) increased tumor inhibition rate (67.54 ± 2.72%) and the amount of apoptotic cells. As confirmed by FT-IR and NMR, the partial protonation of OILs were demonstrated to have high hydrogen bond forming capacity, thus showing low polarity and good biocompatibility. More importantly, based on C-NMR study, OILs demonstrated higher hydrogen bond forming capacity, and formed bridge between drug ion-pair (O-H of counter-ion) and PVA (O-H), increased the molecular mobility of PVA, thus maintaining a long drug release capacity. Therefore, an imatinib FFS was developed with good therapeutic effect and the effect of drug ion-pair and OILs on increasing the drug skin retention and controlled release of imatinib FFS for topical therapy was clarified at the molecular level, which provided a safe and effective way for the treatment of cutaneous melanoma.

摘要

基于药物离子对和新设计的低聚离子液体(OILs)开发了一种伊马替尼控释成膜系统(FFS),用于皮肤黑色素瘤的局部治疗,该系统避免了口服给药的全身副作用,并维持了长期的局部治疗效果。OILs显著提高了药物释放能力约1.5倍,以及FFS的可成型性和稳定性(通过原子力显微镜/偏光显微镜验证)。对荷黑色素瘤小鼠的体内抗肿瘤疗效研究表明,与口服胶囊相比,局部应用优化后的伊马替尼FFS显著(p < 0.01)提高了肿瘤抑制率(67.54 ± 2.72%)和凋亡细胞数量。傅里叶变换红外光谱和核磁共振证实,OILs的部分质子化具有高氢键形成能力,因此显示出低极性和良好的生物相容性。更重要的是,基于碳核磁共振研究,OILs表现出更高的氢键形成能力,并在药物离子对(抗衡离子的O-H)和聚乙烯醇(O-H)之间形成桥梁,增加了聚乙烯醇的分子流动性,从而维持了长期的药物释放能力。因此,开发了一种具有良好治疗效果的伊马替尼FFS,并在分子水平上阐明了药物离子对和OILs对提高伊马替尼FFS皮肤药物保留率和控释的作用,为皮肤黑色素瘤的治疗提供了一种安全有效的方法。

相似文献

1
Construction of Imatinib Controlled Release Film-Forming System Based on Drug Ion-Pair and Oligomeric Ionic Liquids for the Long Local Therapy of Cutaneous Melanoma.基于药物离子对和低聚离子液体构建伊马替尼控释成膜系统用于皮肤黑色素瘤的长效局部治疗
AAPS PharmSciTech. 2023 Mar 25;24(4):87. doi: 10.1208/s12249-023-02546-3.
2
Molecular mechanism of ion-pair releasing from acrylic pressure sensitive adhesive containing carboxyl group: Roles of doubly ionic hydrogen bond in the controlled release process of bisoprolol ion-pair.含羧基丙烯酸压敏胶中离子对释放的分子机制:双离子氢键在比索洛尔离子对控制释放过程中的作用。
J Control Release. 2018 Nov 10;289:146-157. doi: 10.1016/j.jconrel.2018.09.024. Epub 2018 Sep 28.
3
Development of gliclazide ionic liquid and the transdermal patches: An effective and noninvasive sustained release formulation to achieve hypoglycemic effects.格列齐特离子液体和透皮贴剂的研制:一种有效且无创的持续释放制剂,可实现降血糖效果。
Eur J Pharm Sci. 2021 Sep 1;164:105915. doi: 10.1016/j.ejps.2021.105915. Epub 2021 Jun 17.
4
Ionic liquid-mediated delivery of a BCL-2 inhibitor for topical treatment of skin melanoma.离子液体介导的 BCL-2 抑制剂传递用于皮肤黑色素瘤的局部治疗。
J Control Release. 2022 Sep;349:783-795. doi: 10.1016/j.jconrel.2022.07.035. Epub 2022 Aug 2.
5
Investigate the control release effect of ion-pair in the development of escitalopram transdermal patch using FT-IR spectroscopy, molecular modeling and thermal analysis.利用傅里叶变换红外光谱(FT-IR)、分子模拟和热分析研究离子对在艾司西酞普兰透皮贴剂研发中的控释效果。
Int J Pharm. 2017 Aug 30;529(1-2):391-400. doi: 10.1016/j.ijpharm.2017.06.089. Epub 2017 Jun 30.
6
Enhanced Drug Loading in the Drug-in-Adhesive Transdermal Patch Utilizing a Drug-Ionic Liquid Strategy: Insight into the Role of Ionic Hydrogen Bonding.利用药物离子液体策略增强药物贴剂中的药物载药量:离子氢键作用的作用机制研究。
Mol Pharm. 2021 Mar 1;18(3):1157-1166. doi: 10.1021/acs.molpharmaceut.0c01054. Epub 2021 Jan 28.
7
Formulation considerations in the design of topical, polymeric film-forming systems for sustained drug delivery to the skin.用于向皮肤持续给药的局部用聚合物成膜系统设计中的制剂考量
Eur J Pharm Biopharm. 2015 Apr;91:9-15. doi: 10.1016/j.ejpb.2015.01.002. Epub 2015 Jan 14.
8
Layer-by-layer polymer coated gold nanoparticles for topical delivery of imatinib mesylate to treat melanoma.用于甲磺酸伊马替尼局部递送以治疗黑色素瘤的逐层聚合物包覆金纳米颗粒。
Mol Pharm. 2015 Mar 2;12(3):878-88. doi: 10.1021/mp5007163. Epub 2015 Jan 27.
9
Imatinib mesylate inhibits platelet-derived growth factor receptor phosphorylation of melanoma cells but does not affect tumorigenicity in vivo.甲磺酸伊马替尼抑制黑色素瘤细胞的血小板衍生生长因子受体磷酸化,但不影响其体内致瘤性。
J Invest Dermatol. 2004 Feb;122(2):400-5. doi: 10.1046/j.0022-202X.2004.22231.x.
10
Film-Forming Systems for the Delivery of DNDI-0690 to Treat Cutaneous Leishmaniasis.用于递送DNDI-0690治疗皮肤利什曼病的成膜系统
Pharmaceutics. 2021 Apr 8;13(4):516. doi: 10.3390/pharmaceutics13040516.

本文引用的文献

1
Ionic liquid-mediated delivery of a BCL-2 inhibitor for topical treatment of skin melanoma.离子液体介导的 BCL-2 抑制剂传递用于皮肤黑色素瘤的局部治疗。
J Control Release. 2022 Sep;349:783-795. doi: 10.1016/j.jconrel.2022.07.035. Epub 2022 Aug 2.
2
Physicochemical and biopharmaceutical aspects influencing skin permeation and role of SLN and NLC for skin drug delivery.影响皮肤渗透的物理化学和生物药剂学方面以及固体脂质纳米粒和纳米结构脂质载体在皮肤给药中的作用。
Heliyon. 2022 Feb 11;8(2):e08938. doi: 10.1016/j.heliyon.2022.e08938. eCollection 2022 Feb.
3
Insulin Transdermal Delivery System for Diabetes Treatment Using a Biocompatible Ionic Liquid-Based Microemulsion.
用于糖尿病治疗的胰岛素透皮递送系统:基于生物相容离子液体的微乳。
ACS Appl Mater Interfaces. 2021 Sep 15;13(36):42461-42472. doi: 10.1021/acsami.1c11533. Epub 2021 Aug 30.
4
Ion Pairs for Transdermal and Dermal Drug Delivery: A Review.用于经皮和皮肤给药的离子对:综述
Pharmaceutics. 2021 Jun 20;13(6):909. doi: 10.3390/pharmaceutics13060909.
5
Film-Forming Systems for the Delivery of DNDI-0690 to Treat Cutaneous Leishmaniasis.用于递送DNDI-0690治疗皮肤利什曼病的成膜系统
Pharmaceutics. 2021 Apr 8;13(4):516. doi: 10.3390/pharmaceutics13040516.
6
Improving dermal delivery of hyaluronic acid by ionic liquids for attenuating skin dehydration.离子液体改善透明质酸经皮传递以减轻皮肤脱水。
Int J Biol Macromol. 2020 May 1;150:528-535. doi: 10.1016/j.ijbiomac.2020.02.072. Epub 2020 Feb 10.
7
Novel Polyvinyl Alcohol (PVA)/Cellulose Nanocrystal (CNC) Supramolecular Composite Hydrogels: Preparation and Application as Soil Conditioners.新型聚乙烯醇(PVA)/纤维素纳米晶体(CNC)超分子复合水凝胶:作为土壤改良剂的制备与应用
Nanomaterials (Basel). 2019 Oct 1;9(10):1397. doi: 10.3390/nano9101397.
8
Molecular Dynamics and Physical Stability of Pharmaceutical Co-amorphous Systems: Correlation Between Structural Relaxation Times Measured by Kohlrausch-Williams-Watts With the Width of the Glass Transition Temperature (ΔT) and the Onset of Crystallization.药物共无定形系统的分子动力学和物理稳定性:通过 Kohlrausch-Williams-Watts 测量的结构弛豫时间与玻璃化转变温度(ΔT)的宽度和结晶起始的相关性。
J Pharm Sci. 2019 Dec;108(12):3848-3858. doi: 10.1016/j.xphs.2019.09.013. Epub 2019 Sep 19.
9
Synthesis and characterization of choline-fatty-acid-based ionic liquids: A new biocompatible surfactant.胆碱脂肪酸基离子液体的合成与表征:一种新型生物相容性表面活性剂。
J Colloid Interface Sci. 2019 Sep 1;551:72-80. doi: 10.1016/j.jcis.2019.04.095. Epub 2019 May 2.
10
Efficacy Evaluation of Imatinib for the Treatment of Melanoma: Evidence From a Retrospective Study.伊马替尼治疗黑色素瘤的疗效评价:来自回顾性研究的证据。
Oncol Res. 2019 Mar 29;27(4):495-501. doi: 10.3727/096504018X15331163433914. Epub 2018 Aug 3.