Lori Setton - Durham NC, US Ashutosh Chilkoti - Durham NC, US Virginia Kraus - Hillsborough NC, US Helawe Betre - Durham NC, US Matthew Dreher - Durham NC, US
International Classification:
A61K 39/395 A61K 9/14 A61M 31/00
US Classification:
424486000, 424145100, 424078270, 604500000
Abstract:
A method for delivering a drug depot of a compound of interest to a selected region in a subject. The method comprises administering a composition directly to said region of interest, the composition comprising the compound of interest to be delivered (such as an antiinflammatory agent or a chemotherapeutic agent) and a polymer (such as an elastin-like peptide or ELP) that undergoes an inverse temperature phase transition, so that a sustained release of the compound of interest at the selected region is provided. Compositions useful for carrying out the invention are also described.
Drug Delivery With Stimulus Responsive Biopolymers
Ashutosh Chilkoti - Durham NC, US Matthew Robert Dreher - Durham NC, US Daniel Eugene Meyer - Durham NC, US
Assignee:
DUKE UNIVERSITY - Durham NC
International Classification:
A61K 47/48 A61K 49/00 A61K 51/00
US Classification:
424 165, 530402, 5303917, 424 91
Abstract:
The present invention provides conjugate compounds comprising (a) an active compound; (b) optionally, but in some embodiments preferably, an affinity binding agent; and (c) a block copolymer, the block copolymer comprising: (i) a first elastin-like polypeptide having a first Tt and (U) a second elastin-like polypeptide having a second Tt greater than the first Tt. Method for the targeted delivering of an active compound in vivo to a selected region within a subject with such agents are also described.
Elastin-Like Polypeptide And Gadolinium Conjugate For Magnetic Resonance Imaging
Ashutosh Chilkoti - Durham NC, US Matthew R. Dreher - Rockville MD, US Daniel E. Meyer - Rexford NY, US Mark W. Dewhirst - Durham NC, US
Assignee:
Duke University - Durham NC
International Classification:
A61K 49/14 C07K 14/00 A61P 35/00 A61P 9/10
US Classification:
424 934, 530400, 428402
Abstract:
A magnetic resonance imaging (MRI) contrast enhancement agent comprising an elastin-like polypeptide (ELP) and one or more paramagnetic metal ions is disclosed. Also disclosed are methods of preparing ELP MRI contrast enhancement agents, formulations comprising ELP MRI contrast enhancement agents, and methods of using ELP MRI contrast enhancement agents to image biological samples and to image and deliver therapeutic agents to targeted sites in vivo. In some embodiments, the ELP MRI agents can be used in methods related to blood volume determination, in magnetic resonance angiography (MRA), and in vascular transport determinations. The ELP MRI contrast agents can also provide information on the expression of various proteins through affinity targeting or enzymatic crosslinking in order to aid in diagnosis and in the spatial definition of pathologic tissue.
Cyclized Ngr Peptide Compounds, Compositions, And Methods Of Their Use
Bradford J. Wood - Potomac MD, US Matthew Dreher - Rockville MD, US Ayele H. Negussie - Rockville MD, US
International Classification:
A61K 49/00 C07K 7/64 A61K 38/12 A61K 9/127
US Classification:
424 91, 530321, 514 211, 424450
Abstract:
Cyclized peptide compounds containing the NGR motif of formula (I) or a pharmaceutically-acceptable salt thereof are disclosed. Compositions comprising the cyclized peptide compounds and methods of their use are also disclosed.
Methods And Compositions For Modulating Drug-Polymer Architecture, Pharmacokinetics And Biodistribution
Ashutosh Chilkoti - Durham NC, US John A. Mackay - Durham NC, US Matthew R. Dreher - Durham NC, US
International Classification:
A61K 38/16 A61P 35/00 C07K 1/113
US Classification:
514 193, 514 11, 514 212, 530402, 514 209
Abstract:
Drug-polymer chemotherapeutics are provided having improved therapeutic efficacy and reduced dose-limiting toxicity. Methods are also provided for modulating the architecture, pharmacokinetics and biodistribution of drug-polymers and for reducing the dependence of transition temperature on concentration for drug-polymers.
Direct Drug Delivery System Based On Thermally Responsive Biopolymers
Lori A. SETTON - Durham NC, US Ashutosh Chilkoti - Durham NC, US Virginia B. Kraus - Hillsborough NC, US Helawe Betre - Durham NC, US Matthew R. Dreher - Durham NC, US
Assignee:
Duke University - Durham NC
International Classification:
A61K 38/16 A61K 39/395 A61P 19/02
US Classification:
4241341, 514 212, 514 167, 514 168
Abstract:
A method for delivering a drug depot of a compound of interest to a selected region in a subject. The method comprises administering a composition directly to said region of interest, the composition comprising the compound of interest to be delivered (such as an antiinflammatory agent or a chemotherapeutic agent) and a polymer (such as an elastin-like peptide or ELP) that undergoes an inverse temperature phase transition, so that a sustained release of the compound of interest at the selected region is provided. Compositions useful for carrying out the invention are also described.
Ari Ilkka Mikael Partanen - Bethesda MD, US Matthew Robert Dreher - Rockville MD, US Pavel Sergeyevich Yarmolenko - Silver Spring MD, US Antti Johannes Viitala - Espoo, FI Julia Kristina Enholm - Helsingfors, FI Max Oskar Kohler - Espoo, FI
Assignee:
NATIONAL INSTITUTES OF HEALTH - Bethesda MD KONINKLIJKE PHILIPS ELECTRONICS N.V. - EINDHOVEN
International Classification:
A61N 7/00
US Classification:
600 1, 601 2
Abstract:
A therapeutic apparatus () comprising a high intensity focused ultrasound system () for heating a target zone (). The therapeutic apparatus further comprises a magnetic resonance imaging system (). The therapeutic apparatus further comprises a memory () containing machine executable instructions () for execution by a processor (). Execution of the instructions cause the processor to: generate () heating commands () which cause the high intensity focused ultrasound system to sonicate the subject; repeatedly acquire () magnetic resonance data () during execution of the heating commands; repeatedly calculate () a spatially dependent parameter (); and repeatedly modify () the heating commands in accordance with the spatially dependent parameter such that within the target zone the spatially dependent parameter remains below a first predetermined threshold and above a second predetermined threshold.
Matthew R. DREHER - Rockville MD, US Karun V. SHARMA - McLean VA, US Bradford J. WOOD - Bethesda MD, US
Assignee:
MUSC FOUNDATION FOR RESEACH DEVELOPMENT - Charleston SC
International Classification:
A61B 5/0275
US Classification:
600431
Abstract:
Methods for quantitative perfusion analysis for embolotherapy are presented. The method quantitatively measures blood flow changes based on angiographic information. The method may provide potential evaluation of optimal embolization endpoints in vascular vessels. The method may be used in various applications such as transcatheter arterial chemoembolization (TACE), or other medical procedures that affect blow flow within bodily tissues. The method is applicable towards treatment of tumors in liver, kidney, brain, and other organs.