Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Feb 26:13:1139-1158.
doi: 10.2147/IJN.S150205. eCollection 2018.

Design and synthesis of nanoscaled IQCA-TAVV as a delivery system capable of antiplatelet activation, targeting arterial thrombus and releasing IQCA

Affiliations

Design and synthesis of nanoscaled IQCA-TAVV as a delivery system capable of antiplatelet activation, targeting arterial thrombus and releasing IQCA

Jianhui Wu et al. Int J Nanomedicine. .

Abstract

Background: Arterial thrombosis has been associated with a series of pathological conditions, and the discovery of arterial thrombosis inhibitor is of clinical importance.

Methods: By analyzing the pharmacophores of anti-platelet agents, thrombus targeting peptide and anti-thrombotic nano-systems 3S-1,2,3,4-tetrahydroisoquino-line-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val (IQCA-TAVV) was designed and prepared as a nano-scaled arterial thrombosis inhibitor.

Results: In vitro the nanoparticles of IQCA-TAVV were able to adhere onto the surface of activated platelets, attenuate activated platelets to extend pseudopodia and inhibit activated platelets to form aggregators. In vivo IQCA-TAVV targeted arterial thrombus, dose dependently inhibited arterial thrombosis with a 1 nmol/kg of minimal effective dose, and the activity waŝ1670 folds of that of aspirin.

Conclusion: IQCA-TAVV represented the design, preparation and application of nanomedicine capable of adhering on the surface of activated platelets, attenuating platelet activation, targeting arterial thrombus and inhibiting arterial thrombosis.

Keywords: antithrombosis; arterial thrombosis; nanodelivery; thrombus targeting.

PubMed Disclaimer

Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
The combination of pharmacophores of the antiplatelet agents, thrombus-targeting peptide Arg-Gly-Asp-Val and antithrombotic agents leads to the design of IQCA-TAVV as a thrombus-targeting nanodelivery system capable of antiplatelet activation, targeting arterial thrombus and releasing IQCA. Abbreviations: IQCA, 3S-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid; IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val.
Figure 2
Figure 2
FT-MS spectrum, NOESY 2D NMR spectrum and the dimer of IQCA-TAVV. Notes: (A and B) FT-MS spectrum and qCID spectrum of 1 nM solution of IQCA-TAVV in ultrapure water, and the red box shows the amplified region in the MS spectrum; (C) NOESY 2D NMR spectrum of IQCA-TAVV and red ring–labeled interesting cross-peak; (D) Energy-minimized conformation of IQCA-TAVV’s monomer; (E) Energy-minimized conformation of IQCA-TAVV’s dimer. Abbreviations: FT-MS, Fourier transform mass spectrometry; IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val; Intens, intensities; NMR, nuclear magnetic resonance; qCID, qualitative contingent influence diagram.
Figure 3
Figure 3
TEM and SEM images, as well as mesoscale simulation software-predicted nanoparticle of IQCA-TAVV. Notes: (A) TEM image of 10 nM IQCA-TAVV in ultrapure water; (B) TEM image of 0.1 nM IQCA-TAVV in ultrapure water; (C) Particle size distribution of TEM image of 0.1 nM IQCA-TAVV in ultrapure water; (D) SEM image of lyophilized powders from 10 nM IQCA-TAVV in ultrapure water; (E) Particle size distribution of TEM image of lyophilized powders from 10 nM IQCA-TAVV in ultrapure water; (F) Mesoscale simulation software-predicted nanoparticle of IQCA-TAVV. Abbreviations: IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val; TEM, transmission electron microscopy; SEM, scanning electron microscopy.
Figure 4
Figure 4
Tyndall effect, zeta potential and size of IQCA-TAVV in ultrapure water. Notes: (A) Ultrapure water without radiation; (B) ultrapure water with 650 nm laser radiation; (C) IQCA-TAVV in pH 6.7 ultrapure water (1 nM) with 650 nm laser radiation; (D) IQCA-TAVV in pH 1.2 ultrapure water (1 nM) with 650 nm laser radiation; (E) IQCA-TAVV in pH 6.7 ultrapure water (10 nM) with 650 nm laser radiation; (F) IQCA-TAVV in pH 1.2 ultrapure water (10 nM) with 650 nm laser radiation; (G) zeta potential of IQCA-TAVV in ultrapure water (10 nM); (H) particle size of 10 nM solution of IQCA-TAVV in normal saline over 7 days (n=6). Abbreviation: IQCA-TAVV, N-(3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-Thr-Ala-Arg-Gly-Asp(Val)-Val.
Figure 5
Figure 5
AFM images of the resting rat platelets and the interaction between nanoparticles of IQCA-TAVV and AA-activated rat platelets. Notes: (A) IC50 of IQCA-TAVV against AA-activated rat platelet aggregation; (B) AFM image of rat plasma without platelets; (C) AFM image of IQCA-TAVV in rat plasma (10 nM) to mirror the feature of the particles in physiologic environment; (D) AFM image of resting platelets without IQCA-TAVV; (E) AFM image of AA-activated platelets without IQCA-TAVV; (F) AFM image of IQCA-TAVV (10 nM)-treated resting platelets; local amplified particle labeled by blue box; (G) AFM image of IQCA-TAVV (100 nM)-treated AA-activated platelets. Besides, the AFM images of normal saline and IQCA-TAVV in normal saline (10 nM) are shown in Figure S5, the height of particle was labeled by red arrow. Abbreviations: IQCA-TAVV, N-(3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-Thr-Ala-Arg-Gly-Asp(Val)-Val; AA, arachidonic acid; AFM, atomic force microscopy.
Figure 6
Figure 6
AFM images of the resting rat platelets and the effect of IQCA-TAVV nanoparticles on TH-activated rat platelets. Notes: (A) IC50 of IQCA-TAVV against TH-induced rat platelet aggregation; (B) AFM image of the resting rat platelets; (C) AFM image of TH-activated rat platelets without IQCA-TAVV; (D) AFM image of TH-activated platelets treated with 0.05 nM of IQCA-TAVV; (E) AFM image of TH-activated platelets treated with 0.5 nM of IQCA-TAVV; (F) AFM image of TH-activated platelets treated with 5 nM of IQCA-TAVV. Abbreviations: IQCA-TAVV, N-(3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-Thr-Ala-Arg-Gly-Asp(Val)-Val; TH, thrombin; AFM, atomic force microscopy.
Figure 7
Figure 7
SEM images of the action of the nanoparticles of IQCA-TAVV on rat platelets. Notes: (A) SEM images of AA-activated rat platelets treated with normal saline, in which an amplified platelet having a smooth surface is inserted and the extended pseudopodia are labeled with red arrowheads; (B) SEM images of AA-activated rat platelets treated with 200 nM IQCA-TAVV, in which an amplified platelet without pseudopodia and the nanoparticles of IQCA-TAVV on the surface are labeled with blue arrowheads. Abbreviations: SEM, scanning electron microscopy; AA, arachidonic acid; IQCA-TAVV, N-(3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-Thr-Ala-Arg-Gly-Asp(Val)-Val.
Figure 8
Figure 8
Anti-arterial thrombosis activities of IQCA-TAVV, n=12. Notes: (A) At 10 nmol/kg dose IQCA-TAVV effectively inhibits the mice forming an arterial thrombus; (B) IQCA-TAVV dose-dependently inhibits the rats forming an arterial thrombus. Abbreviations: IQCA-TAVV, N-(3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-Thr-Ala-Arg-Gly-Asp(Val)-Val; TAVV, Thr-Ala-Arg-Gly-Asp(Val)-Val; NS, normal saline.
Figure 9
Figure 9
ESI(±)-FT-MS spectra of the extract of the organs and thrombus of rats treated with 10 nmol/kg IQCA-TAVV. Notes: (A) ESI(-)-FT-MS spectrum of the thrombus extract; the local amplified inset shows an ion peak at 178.07821, the mass of IQCA subtracting H; (B) ESI(+)-FT-MS spectrum of the thrombus extract; the local amplified inset shows an ion peak at 519.25641, the mass of TARGD plus H; (C) ESI(-)-FT-MS spectrum of the blood extract, the local amplified inset was labeled by red box and shows no ion peak of IQCA; (DI) The local amplified ESI(-)-FT-MS spectra of the extracts of the brain, heart, lung, liver, spleen and kidney; the local amplified insets show no such ion peak of IQCA. Abbreviations: Intens, intensities; ESI, electrospray ionization; FT-MS, Fourier transform mass spectrometry; IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val; TAVV, Thr-Ala-Arg-Gly-Asp(Val)-Val.
Figure 10
Figure 10
Effects of IQCA-TAVV on mouse Cr, ALT and AST, n=5. Notes: (A) Serum Cr of ICR mice treated with NS and 1 μmol/kg of IQCA-TAVV; (B) Serum ALT of ICR mice treated with NS and 1 μmol/kg of IQCA-TAVV; (C) Serum AST of ICR mice treated with NS and 1 μmol/kg of IQCA-TAVV. Abbreviations: ALT/GPT, alanine aminotransferase/glutamic pyruvic transaminase; AST/GOT, aspartate aminotransferase/glutamic oxaloacetic transaminase; Cr, creatinine; NS, normal saline; ICR, institute of Cancer Research.
Figure 11
Figure 11
Hypothesized thrombus-specific release of IQCA and Thr-Ala-Arg-Gly-Asp from IQCA-TAVV. Abbreviations: IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val; IQCA, 3S-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid.
Scheme 1
Scheme 1
Synthetic route to IQCA-TAVV. Notes: (a) HCHO and HCl; (b) (Boc)2O and NaOH; (c) DCC, HOBt, and NMM; (d) 2N NaOH and methanol; (e) Hydrogen chloride in ethyl acetate (4N); (f) CF3CO2H/CF3SO3H. Abbreviations: IQCA-TAVV, 3S-1,2,3,4-tetrahydroisoquinoline-3-carbonyl-Thr-Ala-Arg-Gly-Asp(Val)-Val; DCC, dicyclohexylcarbodiimide; HOBt, N-hydroxybenzotriazole; NMM, N-methylmorpholine.

Similar articles

Cited by

References

    1. Agnello L, Bivona G, Lo Sasso B, et al. Galectin-3 in acute coronary syndrome. Clin Biochem. 2017;50(13–14):797–803. - PubMed
    1. Asrar ul Haq M, Erickson M, Rankin J, Whelan A. Late strut fracture within a partially resorbed bioresorbable vascular scaffold: a possible cause of late scaffold thrombosis and acute coronary syndrome. Heart Lung Circ. 2017;26(4):e26–e28. - PubMed
    1. Laine M, Frere C, Cuisset T, et al. Potential mechanism of acute stent thrombosis with bivalirudin following percutaneous coronary intervention in acute coronary syndromes. Int J Cardiol. 2016;220:496–500. - PubMed
    1. deVeber GA, Kirton A, Booth FA, et al. Epidemiology and outcomes of arterial ischemic stroke in children: the Canadian pediatric ischemic stroke registry. Pediatr Neurol. 2017;69:58–70. - PubMed
    1. Arnaez J, Garcia-Alix A. Extracerebral thrombosis in symptomatic neonatal arterial ischemic stroke. Eur J Pediatr Neurol. 2017;21(4):687–688. - PubMed

MeSH terms