针对逼尿肌过度活动和间质性膀胱炎/膀胱疼痛综合征的膀胱内脂质体和反义治疗。

ISRN Pharmacology Pub Date : 2014-01-15 eCollection Date: 2014-01-01 DOI:10.1155/2014/601653
Pradeep Tyagi, Mahendra P Kashyap, Naoki Kawamorita, Tsuyoshi Yoshizawa, Michael Chancellor, Naoki Yoshimura
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引用次数: 0

摘要

目的。膀胱内给药为治疗逼尿肌过度活动和间质性膀胱炎/膀胱疼痛综合征(IC/PBS)带来了更多益处,以下综述将重点介绍膀胱内给药的最新进展。结果。对于间质性膀胱炎/膀胱疼痛综合征(IC/PBS)患者来说,膀胱内给药是限制DMSO等强效药物作用的首选给药途径,而对于逼尿肌过度活动症患者来说,膀胱内给药是限制肉毒杆菌毒素作用的首选给药途径。对口服治疗无效或需要减轻传统给药途径不良反应的患者也会选择这种途径。由于载体(载体)毒性或作用持续时间短,这种药物在某些情况下的作用可能会受到限制。为了克服这些限制,人们正在努力开发用于膀胱内给药生物技术产品(包括反义寡核苷酸)的脂质体平台。结论。采用前瞻性思维方法可以实现药物输送系统的进步,从而在未来改善膀胱疾病的药物治疗。纳米技术领域的最新发展可将这种治疗模式从难治性病例的二线治疗提升到疾病治疗的前沿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intravesical liposome and antisense treatment for detrusor overactivity and interstitial cystitis/painful bladder syndrome.

Intravesical liposome and antisense treatment for detrusor overactivity and interstitial cystitis/painful bladder syndrome.

Intravesical liposome and antisense treatment for detrusor overactivity and interstitial cystitis/painful bladder syndrome.

Intravesical liposome and antisense treatment for detrusor overactivity and interstitial cystitis/painful bladder syndrome.

Purpose. The following review focuses on the recent advancements in intravesical drug delivery, which brings added benefit to the therapy of detrusor overactivity and interstitial cystitis/painful bladder syndrome (IC/PBS). Results. Intravesical route is a preferred route of administration for restricting the action of extremely potent drugs like DMSO for patients of interstitial cystitis/painful bladder syndrome (IC/PBS) and botulinum toxin for detrusor overactivity. Patients who are either refractory to oral treatment or need to mitigate the adverse effects encountered with conventional routes of administration also chose this route. Its usefulness in some cases can be limited by vehicle (carrier) toxicity or short duration of action. Efforts have been underway to overcome these limitations by developing liposome platform for intravesical delivery of biotechnological products including antisense oligonucleotides. Conclusions. Adoption of forward-thinking approaches can achieve advancements in drug delivery systems targeted to future improvement in pharmacotherapy of bladder diseases. Latest developments in the field of nanotechnology can bring this mode of therapy from second line of treatment for refractory cases to the forefront of disease management.

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