Quantitative Determination of 5-Aminoisoquinoline, a PARP-1 Inhibitor by UPLC-MS/MS: In Silico ADME Profile and In Vitro Metabolic Stability Study

Abstract

5-Aminoisoquinoline (5-AIQ) is a water-soluble, potent and selective Poly (ADP-ribose) polymerase 1 (PARP-1) inhibitor, widely used as a biochemical and pharmacological tool to study the inhibitory effect of PARPs enzyme. In this study, a simple, selective and reliable ultra-performance liquid chromatography-tandem mass spectrometry assay has been developed for the quantitative analysis of 5-AIQ in plasma using pantoprazole as an internal standard (IS). Both 5-AIQ and IS were separated on an Acquity CSH18 (2.1 × 100 mm; 1.7 µm) column after chromatographic elution of mobile phase comprising of 10 mM ammonium acetate and acetonitrile (35:65; v/v) at a flow rate of 0.3 mL/min. Electrospray ionization in positive mode was used for sample ionization and precursor to product ion transitions of 145.0 > 91.0; 145.0 > 117.4 for 5-AIQ and 384.0 > 138.1 for IS were used for detection and quantification in multiple reaction monitoring mode. The assay was linear in the concentration range of 1.0 to 666 ng/mL with correlation coefficient of ≥0.995. The precision and bias were within the acceptable limits of ≤12.68% and −8.6 to 5.9%, respectively, with mean recovery of 79.1% from plasma and negligible matrix effects (92.4%). In silico ADME prediction, 5-AIQ showed to be very soluble in water and high gastrointestinal absorption along with blood–brain barrier (BBB) permeability. The validated assay was successfully applied in a metabolic stability study, and 5-AIQ was moderately metabolized by human liver microsomes with an in vitro half-life of 14.5 min and intrinsic clearance of 47.6 µL/min/mg. The validated method can be utilized for future pharmacokinetic and bio-distribution studies.

Special Issue on the Application of Analytical Chemistry in Pharmaceutical and Biomedicine

“…Wani et al described the spectrofluorometric method along with a computation approach for studying the binding interaction of flavonoids (rutin, sinapic acid, and naringenin) with serum albumin in order to investigate its possible impact on the pharmacokinetics of erlotinib (tyrosine kinase inhibitor (TKI)) in cancer patients [3]. Iqbal et al reported a sensitive UPLC-MS/MS method for the quantitative analysis of 5-aminoisoquinoline (a PARP-1 inhibitor) in biological fluids and established its in silico ADME profile and in vitro stability [4]. Similarly, Ali et al established a precise and eco-friendly approach for the determination of a novel TKI (erdafitinib) in human plasma samples through a validated UPLC-MS/MS method, and the developed assay was further applied in metabolic stability studies [5].…”