Sökning: WFRF:(Hussain Firasat)
> (2021) >
5-HT1A targeting PA...
5-HT1A targeting PARCEST agent DO3AM-MPP with potential for receptor imaging : Synthesis, physico-chemical and MR studies
-
- Chaturvedi, Shubhra (författare)
- Def Res & Dev Org, Div Cyclotron & Radiopharmaceut Sci, Inst Nucl Med & Allied Sci, Brig SK Mazumdar Rd, Delhi 110054, India.
-
- Chaudhary, Vishakha (författare)
- Univ Delhi, Dept Chem, North Campus, Delhi 110007, India.;Def Res & Dev Org, Div Cyclotron & Radiopharmaceut Sci, Inst Nucl Med & Allied Sci, Brig SK Mazumdar Rd, Delhi 110054, India.
-
- Pant, Pradeep (författare)
- Indian Inst Technol, Dept Chem, New Delhi 110016, India.
-
visa fler...
-
- Jha, Preeti (författare)
- Uppsala universitet,Medicinsk strålningsvetenskap
-
- Kumaran, Senthil S. (författare)
- All India Inst Med Sci, New Delhi 110029, India.
-
- Hussain, Firasat (författare)
- Univ Delhi, Dept Chem, North Campus, Delhi 110007, India.
-
- Mishra, Anil Kumar (författare)
- Def Res & Dev Org, Div Cyclotron & Radiopharmaceut Sci, Inst Nucl Med & Allied Sci, Brig SK Mazumdar Rd, Delhi 110054, India.
-
visa färre...
-
Univ Delhi, Dept Chem, North Campus, Delhi 110007, India; Def Res & Dev Org, Div Cyclotron & Radiopharmaceut Sci, Inst Nucl Med & Allied Sci, Brig SK Mazumdar Rd, Delhi 110054, India. Def Res & Dev Org, Div Cyclotron & Radiopharmaceut Sci, Inst Nucl Med & Allied Sci, Brig SK Mazumdar Rd, Delhi 110054, India. (creator_code:org_t)
- Elsevier, 2021
- 2021
- Engelska.
-
Ingår i: Bioorganic chemistry. - : Elsevier. - 0045-2068. ; 106
- Relaterad länk:
-
https://urn.kb.se/re...
-
visa fler...
-
https://doi.org/10.1...
-
visa färre...
Abstract
Ämnesord
Stäng
- Contrast enhancement in MRI using magnetization or saturation transfer techniques promises better sensitivity, and faster acquisition compared to T-1 or T-2 contrast. This work reports the synthesis and evaluation of 5-HT1A targeted PARACEST MRI contrast agent using 1,4,7,10-tetraazacycloDOdecane-4,7,10-triacetAMide (DO3AM) as the bifunctional chelator, and 5-HT1A-antagonist methoxyphenyl piperazine (MPP) as a targeting unit. The multistep synthesis led to the MPP conjugated DO3AM with 60% yield. CEST-related physicochemical parameters were evaluated after loading DO3AM-MPP with paramagnetic MRI active lanthanides: Gadolinium (Gd-DO3AM-MPP) and Europium (Eu-DO3AM-MPP). Luminescence lifetime measurements with Eu-DO3AM-MPP and computational DFT studies using Gd-DO3AM-MPP revealed the coordination of one water molecule (q = 1.43) with metal-water distance (r(M)-H2O) of 2.7 angstrom and water residence time (tau(m)) of 0.23 ms. The dissociation constant of K-d 62 +/- 0.02 pM as evaluated from fluorescence quenching of 5-HT1A (protein) and docking score of -4.81 in theoretical evaluation reflect the binding potential of the complex Gd-DO3AM-MPP with the receptor 5-HT1A. Insights of the docked pose reflect the importance of NH2 (amide) and aromatic ring in Gd-DO3AM-MPP while interacting with Ser 374 and Phe 370 in the antagonist binding pocket of 5-HT1A. Gd-DO3AM-MPP shows longitudinal relaxivity 5.85 mM(-1)s(-1) with a water residence lifetime of 0.93 ms in hippocampal homogenate containing 5-HT1A. The potentiometric titration of DO3AM-MPP showed strong selectivity for Gd3+ over physiological metal ions such as Zn2+ and Cu2+. The in vitro and in vivo studies confirmed the minimal cytotoxicity and presential binding of Gd-DO3AM-MPP with 5-HT1A receptor in the hippocampus region of the mice. Summarizing, the complex Gd-DO3AM-MPP can have a potential for CEST imaging of 5-HT1A receptors.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
Nyckelord
- Chemical Exchange Saturation Transfer
- Computational Studies
- Density Functional Theory
- Water Residence Lifetime
- Longitudinal and Transverse relaxivity
- Fluorescence quenching
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
Till lärosätets databas