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In vivo monitoring of tissue pharmacokinetics of liposome/drug using MRI: Illustration of targeted delivery
Author(s) -
Viglianti Benjamin L.,
Abraham Sheela A.,
Michelich Charles R.,
Yarmolenko Pavel S.,
MacFall James R.,
Bally Marcel B.,
Dewhirst Mark W.
Publication year - 2004
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.20074
Subject(s) - liposome , in vivo , drug delivery , pharmacokinetics , drug , doxorubicin , distribution (mathematics) , chemistry , in vitro , pharmacology , targeted drug delivery , biomedical engineering , medicine , chemotherapy , surgery , biochemistry , biology , mathematical analysis , microbiology and biotechnology , organic chemistry , mathematics
The purpose of this study was to determine if MnSO 4 /doxorubicin (DOX) loaded liposomes could be used for in vivo monitoring of liposome concentration distribution and drug release using MRI. In vitro results show that T 1 shortening correlates with MnSO 4 concentration. Using a temperature‐sensitive liposome formulation, it was found that MnSO 4 release significantly shortened T 1 . This feature, therefore, suggests that content release can also be measured with these MnSO 4 ‐loaded liposomes. The feasibility of monitoring this drug delivery and release‐imaging agent was shown in a murine tumor model. Upon tumor heating, nonthermally sensitive liposomes selectively but heterogeneously accumulated in the tumor region. The thermally sensitive liposomes showed a clear pattern of accumulation at the periphery of the tumor, concordant with the release temperature of this formulation (39–40°C). This liposome contrast agent has potential for use with hyperthermia by providing individualized monitoring of tissue drug concentration distribution during or after treatment. This would allow for: 1) modification of treatment variables to improve the uniformity of drug delivery, and 2) provide a means to select patients most likely to benefit from this liposomal drug treatment. Additionally, the drug‐loading method used for this liposome is applicable to a wide range of drugs, thereby broadening its applicability. The method is also applicable to other liposomal formulations with triggered release mechanisms. Magn Reson Med 51:1153–1162, 2004. © 2004 Wiley‐Liss, Inc.