Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery

Ultrasound (US) increases efficacy of drugs delivered from micelles, but the pharmacokinetics have not been studied previously. In this study, US was used to deliver doxorubicin (Dox) sequestered in micelles in an in vivo rat model with bilateral leg tumors. One of two frequencies with identical mec...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Staples, Bryant J. (author)
مؤلفون آخرون: Pitt, William G. (author), Roeder, Beverly L. (author), Husseini, Ghaleb (author), Rajeev, Deepthi (author), Schaalje, G. Bruce (author)
التنسيق: article
منشور في: 2010
الموضوعات:
الوصول للمادة أونلاين:http://hdl.handle.net/11073/21284
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
_version_ 1864513438452023296
author Staples, Bryant J.
author2 Pitt, William G.
Roeder, Beverly L.
Husseini, Ghaleb
Rajeev, Deepthi
Schaalje, G. Bruce
author2_role author
author
author
author
author
author_facet Staples, Bryant J.
Pitt, William G.
Roeder, Beverly L.
Husseini, Ghaleb
Rajeev, Deepthi
Schaalje, G. Bruce
author_role author
dc.creator.none.fl_str_mv Staples, Bryant J.
Pitt, William G.
Roeder, Beverly L.
Husseini, Ghaleb
Rajeev, Deepthi
Schaalje, G. Bruce
dc.date.none.fl_str_mv 2010
2021-01-26T09:03:42Z
2021-01-26T09:03:42Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv Staples BJ, Pitt WG, Roeder BL, Husseini GA, Rajeev D, Schaalje GB. Distribution of doxorubicin in rats undergoing ultrasonic drug delivery. J Pharm Sci. 2010 Jul;99(7):3122-31. doi: 10.1002/jps.22088. PMID: 20166203; PMCID: PMC4533826.
0022-3549
http://hdl.handle.net/11073/21284
10.1002/jps.22088
dc.language.none.fl_str_mv en_US
dc.publisher.none.fl_str_mv Elsevier
dc.relation.none.fl_str_mv https://doi.org/10.1002/jps.22088
dc.subject.none.fl_str_mv Ultrasound
Drug delivery
Doxorubicin
Rat tumor model
Pharmacokinetics
dc.title.none.fl_str_mv Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
dc.type.none.fl_str_mv Peer-Reviewed
Postprint
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Ultrasound (US) increases efficacy of drugs delivered from micelles, but the pharmacokinetics have not been studied previously. In this study, US was used to deliver doxorubicin (Dox) sequestered in micelles in an in vivo rat model with bilateral leg tumors. One of two frequencies with identical mechanical index and intensity was delivered for 15 min to one tumor immediately after systemic injection of micellar Dox. Pharmacokinetics in myocardium, liver, skeletal muscle, and tumors were measured for 1 week. When applied in combination with micellar Dox, the ultrasoincated tumor had higher Dox concentrations at 30 min, compared to bilateral noninsonated controls. Initially, concentrations were highest in heart and liver, but within 24 h they decreased significantly. From 24 h to 7 days, concentrations remained highest in tumors, regardless of whether they received US or not. Comparison of insonated and noninsonated tumors showed 50% more Dox in the insonated tumor at 30 min posttreatment. Four weekly treatment produced additional Dox accumulation in the myocardium but not in liver, skeletal leg muscle, or tumors compared to single treatment. Controls showed that neither US nor the empty carrier impacted tumor growth. This study shows that US causes more release of drug at the targeted tumor. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:3122–3131, 2010
format article
id aus_44dd45baed86c0be577a54b2eb3d830a
identifier_str_mv Staples BJ, Pitt WG, Roeder BL, Husseini GA, Rajeev D, Schaalje GB. Distribution of doxorubicin in rats undergoing ultrasonic drug delivery. J Pharm Sci. 2010 Jul;99(7):3122-31. doi: 10.1002/jps.22088. PMID: 20166203; PMCID: PMC4533826.
0022-3549
10.1002/jps.22088
language_invalid_str_mv en_US
network_acronym_str aus
network_name_str aus
oai_identifier_str oai:repository.aus.edu:11073/21284
publishDate 2010
publisher.none.fl_str_mv Elsevier
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
spelling Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug DeliveryStaples, Bryant J.Pitt, William G.Roeder, Beverly L.Husseini, GhalebRajeev, DeepthiSchaalje, G. BruceUltrasoundDrug deliveryDoxorubicinRat tumor modelPharmacokineticsUltrasound (US) increases efficacy of drugs delivered from micelles, but the pharmacokinetics have not been studied previously. In this study, US was used to deliver doxorubicin (Dox) sequestered in micelles in an in vivo rat model with bilateral leg tumors. One of two frequencies with identical mechanical index and intensity was delivered for 15 min to one tumor immediately after systemic injection of micellar Dox. Pharmacokinetics in myocardium, liver, skeletal muscle, and tumors were measured for 1 week. When applied in combination with micellar Dox, the ultrasoincated tumor had higher Dox concentrations at 30 min, compared to bilateral noninsonated controls. Initially, concentrations were highest in heart and liver, but within 24 h they decreased significantly. From 24 h to 7 days, concentrations remained highest in tumors, regardless of whether they received US or not. Comparison of insonated and noninsonated tumors showed 50% more Dox in the insonated tumor at 30 min posttreatment. Four weekly treatment produced additional Dox accumulation in the myocardium but not in liver, skeletal leg muscle, or tumors compared to single treatment. Controls showed that neither US nor the empty carrier impacted tumor growth. This study shows that US causes more release of drug at the targeted tumor. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:3122–3131, 2010Elsevier2021-01-26T09:03:42Z2021-01-26T09:03:42Z2010Peer-ReviewedPostprintinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfStaples BJ, Pitt WG, Roeder BL, Husseini GA, Rajeev D, Schaalje GB. Distribution of doxorubicin in rats undergoing ultrasonic drug delivery. J Pharm Sci. 2010 Jul;99(7):3122-31. doi: 10.1002/jps.22088. PMID: 20166203; PMCID: PMC4533826.0022-3549http://hdl.handle.net/11073/2128410.1002/jps.22088en_UShttps://doi.org/10.1002/jps.22088oai:repository.aus.edu:11073/212842024-08-22T12:06:19Z
spellingShingle Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
Staples, Bryant J.
Ultrasound
Drug delivery
Doxorubicin
Rat tumor model
Pharmacokinetics
status_str publishedVersion
title Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
title_full Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
title_fullStr Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
title_full_unstemmed Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
title_short Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
title_sort Distribution of Doxorubicin in Rats Undergoing Ultrasonic Drug Delivery
topic Ultrasound
Drug delivery
Doxorubicin
Rat tumor model
Pharmacokinetics
url http://hdl.handle.net/11073/21284