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Novel pharmaceutical salts of albendazole

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.199515551openalex-snapshot

Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals

inferredcites →https://doi.org/10.1002/jps.21164openalex-snapshot

Synthesis and Characterization of a New Mebendazole Salt: Mebendazole Hydrochloride

inferredcites →https://doi.org/10.1002/jps.22072openalex-snapshot

Enantiotropically Related Albendazole Polymorphs

inferredcites →https://doi.org/10.1002/jps.23658openalex-snapshot

Mebendazole Mesylate Monohydrate: A New Route to Improve the Solubility of Mebendazole Polymorphs

inferredcites →https://doi.org/10.1007/bf01041557openalex-snapshot

Enhanced water-solubility of albendazole by hydroxypropyl-?-cyclodextrin complexation

inferredcites →https://doi.org/10.1007/bf02228633openalex-snapshot

Pharmacokinetics of fenbendazole, albendazole and oxfendazole in sheep

inferredcites →https://doi.org/10.1007/s00280-004-0927-6openalex-snapshot

Antitumor activity of albendazole against the human colorectal cancer cell line HT-29: in vitro and in a xenograft model of peritoneal carcinomatosis

inferredcites →https://doi.org/10.1007/s10947-006-0049-6openalex-snapshot

Crystal and molecular structure of N-(benzylimidazolyl-2)-O-methylcarbamate salts

inferredcites →https://doi.org/10.1016/0022-2860(72)85016-6openalex-snapshot

Spectrometric identification of organic compounds

inferredcites →https://doi.org/10.1016/0378-5173(96)04586-3openalex-snapshot

Preparation, dissolution and characterization of albendazole solid dispersions

inferredcites →https://doi.org/10.1016/j.vibspec.2004.06.001openalex-snapshot

Infrared studies of the thermal conversion of mefenamic acid between polymorphic states

inferredcites →https://doi.org/10.1021/acs.cgd.7b01807openalex-snapshot

A New Thermodynamically Favored Flubendazole/Maleic Acid Binary Crystal Form: Structure, Energetics, and in Silico PBPK Model-Based Investigation

inferredcites →https://doi.org/10.1021/acs.cgd.8b00203openalex-snapshot

Characterization of Pharmaceutical Cocrystals and Salts by Dynamic Nuclear Polarization-Enhanced Solid-State NMR Spectroscopy

inferredcites →https://doi.org/10.1021/cg200008zopenalex-snapshot

On the Track of New Multicomponent Gabapentin Crystal Forms: Synthon Competition and pH Stability

inferredcites →https://doi.org/10.1021/cg200492wopenalex-snapshot

Solubility Advantage of Amorphous Drugs and Pharmaceutical Cocrystals

inferredcites →https://doi.org/10.1021/cg8007014openalex-snapshot

Solid-State NMR Analysis of Organic Cocrystals and Complexes

inferredcites →https://doi.org/10.1021/cg801145copenalex-snapshot

Synthon Competition and Cooperation in Molecular Salts of Hydroxybenzoic Acids and Aminopyridines

inferredcites →https://doi.org/10.1021/ed039p546openalex-snapshot

Spectrometric identification of organic compounds

inferredcites →https://doi.org/10.1021/ja0541332openalex-snapshot

Solid-State Acid−Base Interactions in Complexes of Heterocyclic Bases with Dicarboxylic Acids: Crystallography, Hydrogen Bond Analysis, and 15N NMR Spectroscopy

inferredcites →https://doi.org/10.1021/ja512817fopenalex-snapshot

Solid Solution Hardening of Molecular Crystals: Tautomeric Polymorphs of Omeprazole

inferredcites →https://doi.org/10.1021/mp060126oopenalex-snapshot

Cocrystal or Salt: Does It Really Matter?

inferredcites →https://doi.org/10.1021/mp0601345openalex-snapshot

The Salt−Cocrystal Continuum: The Influence of Crystal Structure on Ionization State

inferredcites →https://doi.org/10.1021/mp0700108openalex-snapshot

Celecoxib:Nicotinamide Dissociation: Using Excipients To Capture the Cocrystal's Potential

inferredcites →https://doi.org/10.1039/b502484fopenalex-snapshot

A versatile procedure for the identification, description and quantification of structural similarity in molecular crystals

inferredcites →https://doi.org/10.1039/b600753hopenalex-snapshot

Systematic investigation of the relationships between 25 crystal structures containing the carbamazepine molecule or a close analogue: a case study of the XPac method

inferredcites →https://doi.org/10.1039/b700506gopenalex-snapshot

Tautomeric polymorphism in omeprazole

inferredcites →https://doi.org/10.1039/c0ce00428fopenalex-snapshot

New solid forms of artemisinin obtained through cocrystallisation

inferredcites →https://doi.org/10.1039/c2ce25724fopenalex-snapshot

Crystal engineering approach to improve the solubility of mebendazole

inferredcites →https://doi.org/10.1039/c2ce26055gopenalex-snapshot

Acid–base crystalline complexes and the pKa rule

inferredcites →https://doi.org/10.1107/s0021889802022112openalex-snapshot

Single-crystal structure validation with the program PLATON

inferredcites →https://doi.org/10.1107/s0108768189012929openalex-snapshot

Graph-set analysis of hydrogen-bond patterns in organic crystals

inferredcites →https://doi.org/10.1107/s1600536806035549openalex-snapshot

The napsylate salt of carbendazim: 2-(methoxycarbonylamino)benzimidazolium naphthalene-1-sulfonate

inferredcites →https://doi.org/10.1107/s2052252514004229openalex-snapshot

Acemetacin cocrystals and salts: structure solution from powder X-ray data and form selection of the piperazine salt

inferredcites →https://doi.org/10.1590/s0104-66322008000200005openalex-snapshot

Enhancement of solubility of albendazole by complexation with β-cyclodextrin

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4831455openalex-extracted

A Strategy for Enhancing Albendazole Desmotropes Bioavailability: Multicomponent Systems of Maltodextrin and Aspartic Acid

inferred← citeshttps://doi.org/10.1002/ange.202318497openalex-snapshot

Hydrophilic Cocrystals with Water Switched Luminescence

inferred← citeshttps://doi.org/10.1002/anie.202318497openalex-snapshot

Hydrophilic Cocrystals with Water Switched Luminescence

inferred← citeshttps://doi.org/10.1007/s12247-021-09588-9openalex-snapshot

Saturation Solubility and Dissolution Property Improvement of Albendazole by Salt Formation Approach

inferred← citeshttps://doi.org/10.1016/j.cej.2021.129839openalex-snapshot

Energetic compounds based on a new fused triazolo[4,5-d]pyridazine ring: Nitroimino lights up energetic performance

inferred← citeshttps://doi.org/10.1016/j.ejpb.2024.114620openalex-snapshot

Design and evaluation of multicomponent systems as a potential strategy to enhance the pharmaceutical performance of albendazole desmotropes

inferred← citeshttps://doi.org/10.1016/j.ejps.2024.106751openalex-snapshot

Enabling a novel solvent method on Albendazole solid dispersion to improve the in vivo bioavailability

inferred← citeshttps://doi.org/10.1016/j.ijpharm.2024.123855openalex-snapshot

Preparation and characterization of new salts of tioconazole. Comparison of their dissolution performance

inferred← citeshttps://doi.org/10.1016/j.jcou.2021.101505openalex-snapshot

Simultaneous formation of inclusion complex and microparticles containing Albendazole and β-Cyclodextrin by supercritical antisolvent co-precipitation

inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129850openalex-snapshot

Eight salts of 4-dimethylaminopyridine and organic acids by H-bonds and some noncovalent associations

inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131770openalex-snapshot

Seven cocrystals of pyrazinamide and organic acids by H-bonds and some noncovalent associations

inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.132883openalex-snapshot

Determination of the tautomerism of albendazole desmotropes using solution and solid state NMR together with DFT theoretical calculations, both energies and chemical shifts

inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135799openalex-snapshot

Exploration of new solid forms of anti-emetic drug domperidone: Novel salts with enhanced solubility and dissolution

inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136068openalex-snapshot

Synthesis, Hirshfeld atom refinement of crystal structure, and Hirshfeld surface analysis of 5-ethoxycarbonyl-6-methyl-4-(2-(trifluoromethyl)phenyl)-3,4-dihydropyrimidin-2-(1H)-one formic acid monosolvate

inferred← citeshttps://doi.org/10.1016/j.mseb.2023.116351openalex-snapshot

Molecular spectroscopy and optical effect of Albendazole chemical compound behaves as liquid crystal: A theoretical and experimental approach

inferred← citeshttps://doi.org/10.1021/acs.cgd.0c01427openalex-snapshot

Advanced Methodologies for Pharmaceutical Salt Synthesis

inferred← citeshttps://doi.org/10.1021/acs.cgd.0c01444openalex-snapshot

Amino–Imino Tautomerism in the Salt Formation of Albendazole: Hydrobromide and Nitrate Salts

inferred← citeshttps://doi.org/10.1021/acs.cgd.1c00413openalex-snapshot

Pharmaceutical Salts of Fenbendazole with Organic Counterions: Structural Analysis and Solubility Performance

inferred← citeshttps://doi.org/10.1021/acs.cgd.4c01208openalex-snapshot

Multicomponent Crystal Forms of Albendazole for Bioavailability Improvement

inferred← citeshttps://doi.org/10.1021/acs.cgd.9b00348openalex-snapshot

Investigating a Soluble Pharmaceutical Salt: Albendazole Hydrochloride

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.4c00152openalex-snapshot

In Situ Eutectic Formation in a Polymeric Matrix via Hot-Melt Reactive Extrusion and the Use of Partial Least Squares Regression Modeling for Reaction Yield Determination

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.4c01508openalex-snapshot

Sweetening the Deal: Sweetener-Based Ionic Liquid of Albendazole Significantly Enhances Its Solubility and Oral Bioavailability

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.9b00851openalex-snapshot

Enhanced Oral Bioavailability and Anti-Echinococcosis Efficacy of Albendazole Achieved by Optimizing the “Spring” and “Parachute”

inferred← citeshttps://doi.org/10.1021/acsinfecdis.9b00231openalex-snapshot

Improvement of Antialveolar Echinococcosis Efficacy of Albendazole by a Novel Nanocrystalline Formulation with Enhanced Oral Bioavailability

inferred← citeshttps://doi.org/10.1039/d2ce01644copenalex-snapshot

Structural features, dissolution performance and anthelmintic efficacy of multicomponent solid forms of fenbendazole with maleic and oxalic acids

inferred← citeshttps://doi.org/10.1039/d3cc02188bopenalex-snapshot

Reversible interconversion of pharmaceutical salt polymorphs facilitated by mechanical methods

inferred← citeshttps://doi.org/10.1039/d5pm00225gopenalex-snapshot

The ideal duo for salt formation: vinpocetine and tosylic acid

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011031openalex-snapshot

Improvement of Antialveolar echinococcosis efficacy of novel Albendazole-Bile acids Derivatives with Enhanced Oral Bioavailability

inferred← citeshttps://doi.org/10.15212/bioi-2025-0045openalex-snapshot

Drug Delivery and Repurposing Approaches for Albendazole Formulations

inferred← citeshttps://doi.org/10.31016/1998-8435-2026-20-2-310-325openalex-snapshot

Chemical transformations of albendazole during mechanical treatment with carboxylic acids and their cytotoxicity

inferred← citeshttps://doi.org/10.3390/cryst14020133openalex-snapshot

Synthesis, Crystal Structure and Supramolecular Features of Novel 2,4-Diaminopyrimidine Salts

inferred← citeshttps://doi.org/10.3390/ijms23116302openalex-snapshot

Molecular Dynamics Simulation of Association Processes in Aqueous Solutions of Maleate Salts of Drug-like Compounds: The Role of Counterion

inferred← citeshttps://doi.org/10.3390/microbiolres16040077openalex-snapshot

Antiprotozoal Activity and Selectivity Index of Organic Salts of Albendazole and Mebendazole

inferred← citeshttps://doi.org/10.3390/molecules25102386openalex-snapshot

Combined X-ray Crystallographic, IR/Raman Spectroscopic, and Periodic DFT Investigations of New Multicomponent Crystalline Forms of Anthelmintic Drugs: A Case Study of Carbendazim Maleate

inferred← citeshttps://doi.org/10.3390/molecules29153571openalex-snapshot

Improving the Solubility, Stability, and Bioavailability of Albendazole through Synthetic Salts

inferred← citeshttps://doi.org/10.3390/ph16060781openalex-snapshot

Diversity of Solid Forms Promoted by Ball Milling: Characterization and Intrinsic Dissolution Studies of Pioglitazone Hydrochloride and Fluvastatin Sodium Drug–Drug Systems

inferred← citeshttps://doi.org/10.3390/pharmaceutics14112321openalex-snapshot

Crystal Engineering of Ionic Cocrystals Sustained by Azolium···Azole Heterosynthons

inferred← citeshttps://doi.org/10.3390/sym13030425openalex-snapshot

Two Faces of Water in the Formation and Stabilization of Multicomponent Crystals of Zwitterionic Drug-Like Compounds

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