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Elimination of light chain tailing in reducing capillary electrophoresis with sodium dodecyl sulfate analysis of a monoclonal antibody

Electrophoresis, 2022-10, Vol.43 (18-19), p.1850-1858

2022

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An Overview of the Stability and Delivery Challenges of Commercial Nucleic Acid Therapeutics

Pharmaceutics, 2023-04, Vol.15 (4), p.1158

2023

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Current developments of bioanalytical sample preparation techniques in pharmaceuticals

Journal of pharmaceutical analysis, 2022-08, Vol.12 (4), p.517-529

2022

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Secondary Packages cannot Protect Liquid Biopharmaceutical Formulations from Dropping-Induced Degradation

Pharmaceutical research, 2021-08, Vol.38 (8), p.1397-1404

2021

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Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II)

International journal of molecular sciences, 2019-12, Vol.21 (1), p.114

2019

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Characterization of Grinding-Induced Subvisible Particles and Free Radicals in a Freeze-Dried Monoclonal Antibody Formulation

Pharmaceutical research, 2022-02, Vol.39 (2), p.399-410

2022

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Formation of an Unprecedented Impurity during CE-SDS Analysis of a Recombinant Protein

Pharmaceutical research, 2020-11, Vol.37 (11), Article 228

2020

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Analogs of the κ opioid receptor antagonist arodyn cyclized by ring-closing metathesis retain κ opioid receptor affinity, selectivity and κ opioid receptor antagonism

Medicinal chemistry research, 2021-07, Vol.30 (7), p.1397-1407

2021

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Uncommon Peptide Bond Cleavage of Glucagon from a Specific Vendor under near Neutral to Basic Conditions

Pharmaceutical research, 2019-08, Vol.36 (8), p.118-11, Article 118

2019

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Effects of polyol excipient stability during storage and use on the quality of biopharmaceutical formulations

Journal of pharmaceutical analysis, 2022-10, Vol.12 (5), p.774-782

2022

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Effects of Excipients on the Chemical and Physical Stability of Glucagon during Freeze-Drying and Storage in Dried Formulations

Pharmaceutical research, 2012-12, Vol.29 (12), p.3278-3291

2012

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A convenient approach to synthesizing peptide C-terminal N-alkyl amides

Biopolymers, 2011, Vol.96 (6), p.715-722

2011

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Freeze-Dried Biopharmaceutical Formulations are Surprisingly Less Stable than Liquid Formulations during Dropping

Pharmaceutical research, 2022-04, Vol.39 (4), p.795-803

2022

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Characterization and exploration of an artifact in the reducing capillary electrophoresis-sodium dodecyl sulfate analysis of the ‘me-too’ drug zuberitamab related to rituximab

Journal of pharmaceutical and biomedical analysis, 2023-05, Vol.228, p.115347-115347, Article 115347

2023

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Prefilled dual chamber devices (DCDs) – Promising high-quality and convenient drug delivery system

International journal of pharmaceutics, 2021-03, Vol.597, p.120314-120314, Article 120314

2021

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EBRB cascade classifier for imbalanced data via rule weight updating

Knowledge-based systems, 2021-07, Vol.223, p.107010, Article 107010

2021

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Identification and characterization of chemical and physical stability of insulin formulations utilizing degraded glycerol after repeated use and storage

European journal of pharmaceutics and biopharmaceutics, 2022-08, Vol.177, p.147-156

2022

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Effect of Annealing on Visible-Bubble Formation and Stability Profiles of Freeze-Dried High Concentration Omalizumab Formulations

Molecular pharmaceutics, 2024-04, Vol.21 (4), p.1691-1704

2024

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Freeze-Dried Monoclonal Antibody Formulations are Unexpectedly More Prone to Degradation Than Liquid Formulations Under Shaking Stress

Journal of pharmaceutical sciences, 2022-07, Vol.111 (7), p.2134-2138

2022

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Drugability Studies are Keys to the Successful Commercialization of Biotherapeutics

Biomedical & pharmacology journal, 2017, Vol.10 (4), p.1593-1601

2017

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The Effects of Excipients on Freeze-dried Monoclonal Antibody Formulation Degradation and Sub-Visible Particle Formation during Shaking

Pharmaceutical research, 2024-02, Vol.41 (2), p.321-334

2024

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Investigation of an artifact during non-reduced capillary electrophoresis with sodium dodecyl sulfate analysis utilizing N-ethylmaleimide as an alkylation reagent

Analytical biochemistry, 2022-10, Vol.655, p.114833-114833, Article 114833

2022

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Monitoring of low-molecular-weight protein aggregation by CE-SDS as a complementary method to SE-HPLC

Journal of pharmaceutical and biomedical analysis, 2023-09, Vol.234, p.115521-115521, Article 115521

2023

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Effects of Secondary Package on Freeze-Dried Biopharmaceutical Formulation Stability During Dropping

Journal of pharmaceutical sciences, 2021-08, Vol.110 (8), p.2916-2924

2021

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The Osmolality and Hemolysis of High-Concentration Monoclonal Antibody Formulations

Pharmaceutical research, 2024-02, Vol.41 (2), p.281-291

2024

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Elimination of light chain tailing in reducing capillary electrophoresis with sodium dodecyl sulfate analysis of a monoclonal antibody

An Overview of the Stability and Delivery Challenges of Commercial Nucleic Acid Therapeutics

Current developments of bioanalytical sample preparation techniques in pharmaceuticals

Secondary Packages cannot Protect Liquid Biopharmaceutical Formulations from Dropping-Induced Degradation

Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II)

Characterization of Grinding-Induced Subvisible Particles and Free Radicals in a Freeze-Dried Monoclonal Antibody Formulation

Formation of an Unprecedented Impurity during CE-SDS Analysis of a Recombinant Protein

Analogs of the κ opioid receptor antagonist arodyn cyclized by ring-closing metathesis retain κ opioid receptor affinity, selectivity and κ opioid receptor antagonism

Uncommon Peptide Bond Cleavage of Glucagon from a Specific Vendor under near Neutral to Basic Conditions

Effects of polyol excipient stability during storage and use on the quality of biopharmaceutical formulations

Effects of Excipients on the Chemical and Physical Stability of Glucagon during Freeze-Drying and Storage in Dried Formulations

A convenient approach to synthesizing peptide C-terminal N-alkyl amides

Freeze-Dried Biopharmaceutical Formulations are Surprisingly Less Stable than Liquid Formulations during Dropping

Characterization and exploration of an artifact in the reducing capillary electrophoresis-sodium dodecyl sulfate analysis of the ‘me-too’ drug zuberitamab related to rituximab

Prefilled dual chamber devices (DCDs) – Promising high-quality and convenient drug delivery system

EBRB cascade classifier for imbalanced data via rule weight updating

Identification and characterization of chemical and physical stability of insulin formulations utilizing degraded glycerol after repeated use and storage

Effect of Annealing on Visible-Bubble Formation and Stability Profiles of Freeze-Dried High Concentration Omalizumab Formulations

Freeze-Dried Monoclonal Antibody Formulations are Unexpectedly More Prone to Degradation Than Liquid Formulations Under Shaking Stress

Drugability Studies are Keys to the Successful Commercialization of Biotherapeutics

The Effects of Excipients on Freeze-dried Monoclonal Antibody Formulation Degradation and Sub-Visible Particle Formation during Shaking

Investigation of an artifact during non-reduced capillary electrophoresis with sodium dodecyl sulfate analysis utilizing N-ethylmaleimide as an alkylation reagent

Monitoring of low-molecular-weight protein aggregation by CE-SDS as a complementary method to SE-HPLC

Effects of Secondary Package on Freeze-Dried Biopharmaceutical Formulation Stability During Dropping

The Osmolality and Hemolysis of High-Concentration Monoclonal Antibody Formulations

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