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基于定量荧光的内镜探针评估光触发脂质体阿霉素的光通量率依赖性动力学

Fluence Rate-Dependent Kinetics of Light-Triggered Liposomal Doxorubicin Assessed by Quantitative Fluorescence-Based Endoscopic Probe.

作者信息

Rohrbach Daniel J, Carter Kevin A, Luo Dandan, Shao Shuai, Aygun-Sunar Semra, Lovell Jonathan F, Sunar Ulas

机构信息

Agilent Technologies, Winooski, Vermont, VT 05404, USA.

Department of Biomedical Engineering, University at Buffalo, Buffalo, NY 14260, USA.

出版信息

Int J Mol Sci. 2025 Jan 30;26(3):1212. doi: 10.3390/ijms26031212.


DOI:10.3390/ijms26031212
PMID:39940981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11818813/
Abstract

Liposomal doxorubicin (Dox), a treatment option for recurrent ovarian cancer, often suffers from suboptimal biodistribution and efficacy, which might be addressed with precision drug delivery systems. Here, we introduce a catheter-based endoscopic probe designed for multispectral, quantitative monitoring of light-triggered drug release. This tool utilizes red-light photosensitive porphyrin-phospholipid (PoP), which is encapsulated in liposome bilayers to enhance targeted drug delivery. By integrating diffuse reflectance and fluorescence spectroscopy, our approach not only corrects for the effects of tissue optical properties but also ensures accurate drug delivery to deep-seated tumors. Preliminary results validate the probe's effectiveness in controlled settings, highlighting its potential for future clinical adaptation. This study sets the stage for in vivo applications, enabling the exploration of next-generation treatment paradigms for the management of cancer that involve optimizing chemotherapy administration for precision and control.

摘要

脂质体阿霉素(Dox)是复发性卵巢癌的一种治疗选择,但常常存在生物分布和疗效欠佳的问题,而精准给药系统或许可以解决这些问题。在此,我们介绍一种基于导管的内镜探头,其设计用于对光触发药物释放进行多光谱定量监测。该工具利用红光光敏卟啉 - 磷脂(PoP),它被包裹在脂质体双层中以增强靶向给药。通过整合漫反射和荧光光谱,我们的方法不仅校正了组织光学特性的影响,还确保了向深部肿瘤的准确给药。初步结果验证了该探头在可控环境中的有效性,突出了其未来临床应用的潜力。这项研究为体内应用奠定了基础,有助于探索涉及优化化疗给药以实现精准和控制的下一代癌症治疗模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/b4fdb256b131/ijms-26-01212-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/bfcca386abc9/ijms-26-01212-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/ab9da9087888/ijms-26-01212-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/13ed8acc0390/ijms-26-01212-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/30fd6de6d47a/ijms-26-01212-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/a2674cc4205a/ijms-26-01212-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/b4fdb256b131/ijms-26-01212-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/bfcca386abc9/ijms-26-01212-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/ab9da9087888/ijms-26-01212-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/13ed8acc0390/ijms-26-01212-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/30fd6de6d47a/ijms-26-01212-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/a2674cc4205a/ijms-26-01212-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af25/11818813/b4fdb256b131/ijms-26-01212-g006.jpg

相似文献

[1]
Fluence Rate-Dependent Kinetics of Light-Triggered Liposomal Doxorubicin Assessed by Quantitative Fluorescence-Based Endoscopic Probe.

Int J Mol Sci. 2025-1-30

[2]
Fluence rate-dependent kinetics of light-triggered liposomal doxorubicin assessed by quantitative fluorescence-based endoscopic probe.

Res Sq. 2025-1-3

[3]
Fluence rate-dependent kinetics of light-triggered liposomal doxorubicin assessed by quantitative fluorescence-based endoscopic probe.

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[4]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Quantitative Fluorescence Imaging of Chemophototherapy Drug Pharmacokinetics Using Laparoscopic SFDI.

Int J Mol Sci. 2025-6-11

本文引用的文献

[1]
A Potent Cancer Vaccine Adjuvant System for Particleization of Short, Synthetic CD8 T Cell Epitopes.

ACS Nano. 2021-3-23

[2]
Pharmacokinetics and pharmacodynamics of liposomal chemophototherapy with short drug-light intervals.

J Control Release. 2019-1-23

[3]
A dual-channel endoscope for quantitative imaging, monitoring, and triggering of doxorubicin release from liposomes in living mice.

Sci Rep. 2017-11-14

[4]
Assessing daylight & low-dose rate photodynamic therapy efficacy, using biomarkers of photophysical, biochemical and biological damage metrics in situ.

Photodiagnosis Photodyn Ther. 2017-10-14

[5]
Vessel-Targeted Chemophototherapy with Cationic Porphyrin-Phospholipid Liposomes.

Mol Cancer Ther. 2017-7-20

[6]
Optical imaging of tissue obtained by transbronchial biopsies of peripheral lung lesions.

J Thorac Dis. 2017-5

[7]
Beyond the Barriers of Light Penetration: Strategies, Perspectives and Possibilities for Photodynamic Therapy.

Theranostics. 2016-10-23

[8]
Sphingomyelin Liposomes Containing Porphyrin-phospholipid for Irinotecan Chemophototherapy.

Theranostics. 2016-10-1

[9]
Rapid Light-Triggered Drug Release in Liposomes Containing Small Amounts of Unsaturated and Porphyrin-Phospholipids.

Small. 2016-6

[10]
Intraoperative optical assessment of photodynamic therapy response of superficial oral squamous cell carcinoma.

J Biomed Opt. 2016-1

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