Image-guided thermosensitive liposomes for focused ultrasound drug delivery: Using NIRF-labelled lipids and topotecan to visualise the effects of hyperthermia in tumours

JOURNAL OF CONTROLLED RELEASE

卷:280

Article

Centelles, Miguel N.¹  Wright, Michael¹  So, Po-Wah²  Amrahli, Maral¹  Xu, Xiao Yun³  Stebbing, Justin⁴  Miller, Andrew D.⁵  Gedroyc, Wladyslaw⁶  Thanou, Maya¹ 

[1] Kings Coll London, Sch Canc & Pharmaceut Sci, London, England

[2] Kings Coll London, Dept Neuroimaging, London, England

[3] Imperial Coll London, Dept Chem Engn, London, England

[4] Imperial Coll London, Dept Surg & Canc, London, England

[5] Global Acorn Ltd, Temple Rd, London, England

[6] Imperial Coll London, Dept Expt Med, London, England

关键词: Near infrared fluorescence;    MRI;    Imaging;    Focused ultrasound;    Liposomes;    Topotecan;    Localised drug delivery;    Cancer;   

DOI  :  10.1016/j.jconrel.2018.04.047

来源: Elsevier

【 摘 要 】

Image guided drug delivery using imageable thermosensitive liposomes (iTSLs) and high intensity focused ultrasound (FUS or HIFU) has attracted interest as a novel and non-invasive route to targeted delivery of anticancer therapeutics. FUS-induced hyperthermia is used as an externally applied trigger for the release of a drug cargo from within thermosensitive drug carriers. It is suggested that sub-ablative hyperthermia significantly modifies the permeability of tumour vasculature and enhances nanoparticle uptake. Here we describe the preparation and use of magnetic resonance imaging (MRI) and near infrared fluorescence (NIRF) labelled thermosensitive liposomes for imaging and tracking of biodistribution and drug release in a murine cancer model. We prepared iTSLs to encapsulate topotecan (Hycamtin((R))), a chemotherapeutic agent which when released in tumours can be monitored by an increase in its intrinsic drug fluorescence. FUS was applied using feedback via subcutaneously placed fine-wire thermocouples to maintain and monitor hyperthermic temperatures. iTSL accumulation was detected within tumours using NIRF imaging immediately after liposome administration. Mild FUS-induced hyperthermia (3 min at 42 degrees C, 30 min post i.v. administration) greatly enhanced iTSLs uptake. A colocalised enhancement of topotecan fluorescence emission was also observed immediately after application of FUS indicating rapid triggered drug release. The phenomena of increased iTSL accumulation and concomitant topotecan release appeared to be amplified by a second mild hyperthermia treatment applied one hour after the first. MRI in vivo also confirmed enhanced iTSLs uptake due to the FUS treatments. Our imaging results indicate the effects of hyperthermia on the uptake of carriers and drug. FUS-induced hyperthermia combined with real time imaging could be used as a tool for tumour targeted drug delivery.

【 授权许可】

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