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Comparative evaluation of Tc-MBIP-X/[C] MBMP for visualization of 18 kDa translocator protein
An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging. Recently, our group has explored a pharmacophore skeleton acetamidobenzoxazolone for positron emission tomography (PET) and single photon...
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Published in: | New journal of chemistry 2019-07, Vol.43 (28), p.11288-11295 |
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container_issue | 28 |
container_start_page | 11288 |
container_title | New journal of chemistry |
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creator | Srivastava, Pooja Kumari, Neelam Kakkar, Dipti Kaul, Ankur Kumar, Pravir Tiwari, Anjani K |
description | An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging. Recently, our group has explored a pharmacophore skeleton acetamidobenzoxazolone for positron emission tomography (PET) and single photon emission computed tomography (SPECT) applications to target TSPO. 2-(2-(5-Bromo/chloro benzoxazolone)acetamide)-3-(1
H
-indol-3-yl)propionate (MBIP-Br/Cl) were synthesized by using tryptophan methyl ester and compared with 2-[5-(4-methoxyphenyl)-2-oxo-1,3-benzoxazol-3(2
H
)-yl]-
N
-methyl-
N
-phenyl acetamide (MBMP) through tracer techniques. Computational docking showed similar results for MBIP-Br/Cl in comparison to MBMP. Their
ex vivo
and
in vivo
biodistributions were assessed in TSPO-rich organs as well as their release kinetics 0-120 min post injection. The
ex vivo
biodistribution showed a 7 fold higher uptake (5.16%ID per g
vs.
0.72%ID per g) in the heart and a 2.5 fold higher uptake (12.91%ID per g
vs.
4.69%ID per g) in the lungs for
99m
Tc-MBIP-Cl compared to that of
99m
Tc-MBIP-Br at 15 min. These findings demonstrated that
99m
Tc-MBIP-Cl has improved pharmacokinetic properties compared to
99m
Tc-MBIP-Br for SPECT application and is comparable to [
11
C]MBMP.
An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging. |
doi_str_mv | 10.1039/c9nj00180h |
format | article |
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H
-indol-3-yl)propionate (MBIP-Br/Cl) were synthesized by using tryptophan methyl ester and compared with 2-[5-(4-methoxyphenyl)-2-oxo-1,3-benzoxazol-3(2
H
)-yl]-
N
-methyl-
N
-phenyl acetamide (MBMP) through tracer techniques. Computational docking showed similar results for MBIP-Br/Cl in comparison to MBMP. Their
ex vivo
and
in vivo
biodistributions were assessed in TSPO-rich organs as well as their release kinetics 0-120 min post injection. The
ex vivo
biodistribution showed a 7 fold higher uptake (5.16%ID per g
vs.
0.72%ID per g) in the heart and a 2.5 fold higher uptake (12.91%ID per g
vs.
4.69%ID per g) in the lungs for
99m
Tc-MBIP-Cl compared to that of
99m
Tc-MBIP-Br at 15 min. These findings demonstrated that
99m
Tc-MBIP-Cl has improved pharmacokinetic properties compared to
99m
Tc-MBIP-Br for SPECT application and is comparable to [
11
C]MBMP.
An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c9nj00180h</identifier><language>eng</language><ispartof>New journal of chemistry, 2019-07, Vol.43 (28), p.11288-11295</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Srivastava, Pooja</creatorcontrib><creatorcontrib>Kumari, Neelam</creatorcontrib><creatorcontrib>Kakkar, Dipti</creatorcontrib><creatorcontrib>Kaul, Ankur</creatorcontrib><creatorcontrib>Kumar, Pravir</creatorcontrib><creatorcontrib>Tiwari, Anjani K</creatorcontrib><title>Comparative evaluation of Tc-MBIP-X/[C] MBMP for visualization of 18 kDa translocator protein</title><title>New journal of chemistry</title><description>An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging. Recently, our group has explored a pharmacophore skeleton acetamidobenzoxazolone for positron emission tomography (PET) and single photon emission computed tomography (SPECT) applications to target TSPO. 2-(2-(5-Bromo/chloro benzoxazolone)acetamide)-3-(1
H
-indol-3-yl)propionate (MBIP-Br/Cl) were synthesized by using tryptophan methyl ester and compared with 2-[5-(4-methoxyphenyl)-2-oxo-1,3-benzoxazol-3(2
H
)-yl]-
N
-methyl-
N
-phenyl acetamide (MBMP) through tracer techniques. Computational docking showed similar results for MBIP-Br/Cl in comparison to MBMP. Their
ex vivo
and
in vivo
biodistributions were assessed in TSPO-rich organs as well as their release kinetics 0-120 min post injection. The
ex vivo
biodistribution showed a 7 fold higher uptake (5.16%ID per g
vs.
0.72%ID per g) in the heart and a 2.5 fold higher uptake (12.91%ID per g
vs.
4.69%ID per g) in the lungs for
99m
Tc-MBIP-Cl compared to that of
99m
Tc-MBIP-Br at 15 min. These findings demonstrated that
99m
Tc-MBIP-Cl has improved pharmacokinetic properties compared to
99m
Tc-MBIP-Br for SPECT application and is comparable to [
11
C]MBMP.
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H
-indol-3-yl)propionate (MBIP-Br/Cl) were synthesized by using tryptophan methyl ester and compared with 2-[5-(4-methoxyphenyl)-2-oxo-1,3-benzoxazol-3(2
H
)-yl]-
N
-methyl-
N
-phenyl acetamide (MBMP) through tracer techniques. Computational docking showed similar results for MBIP-Br/Cl in comparison to MBMP. Their
ex vivo
and
in vivo
biodistributions were assessed in TSPO-rich organs as well as their release kinetics 0-120 min post injection. The
ex vivo
biodistribution showed a 7 fold higher uptake (5.16%ID per g
vs.
0.72%ID per g) in the heart and a 2.5 fold higher uptake (12.91%ID per g
vs.
4.69%ID per g) in the lungs for
99m
Tc-MBIP-Cl compared to that of
99m
Tc-MBIP-Br at 15 min. These findings demonstrated that
99m
Tc-MBIP-Cl has improved pharmacokinetic properties compared to
99m
Tc-MBIP-Br for SPECT application and is comparable to [
11
C]MBMP.
An elevated translocator protein (18 kDa, TSPO) density is observed during inflammation in the brain and peripheral organs making it a viable target for imaging.</abstract><doi>10.1039/c9nj00180h</doi><tpages>8</tpages></addata></record> |
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source | Royal Society of Chemistry |
title | Comparative evaluation of Tc-MBIP-X/[C] MBMP for visualization of 18 kDa translocator protein |
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