(januari 2004). Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients. The Journal of Antimicrobial Chemotherapy53 (1): 4–9. PMID14657084. DOI: 10.1093/jac/dkh029.
(juni 2001). Ritonavir: an extraordinary example of conformational polymorphism. Pharmaceutical Research18 (6): 859–866. PMID11474792. DOI: 10.1023/A:1011052932607.
(maart 2003). Elucidation of crystal form diversity of the HIV protease inhibitor ritonavir by high-throughput crystallization. Proceedings of the National Academy of Sciences of the United States of America100 (5): 2180–2184. PMID12604798. PMC151315. DOI: 10.1073/pnas.0437744100.
(1 februari 2006). Crystal dissolution kinetics and Gibbs free energy. Journal of Electron Spectroscopy and Related Phenomena150 (2): 248–259. DOI: 10.1016/j.elspec.2005.06.007.
(februari 2017). A Newly Discovered Racemic Compound of Pioglitazone Hydrochloride Is More Stable than the Commercial Conglomerate. Crystal Growth & Design17 (2): 414–417. PMID31537981. PMC6752731. DOI: 10.1021/acs.cgd.6b01638.
(mei 2020). A Trial of Lopinavir-Ritonavir in Adults Hospitalized with Severe Covid-19. The New England Journal of Medicine382 (19): 1787–1799. PMID32187464. PMC7121492. DOI: 10.1056/NEJMoa2001282.
(oktober 2020). Molecular dynamics analysis predicts ritonavir and naloxegol strongly block the SARS-CoV-2 spike protein-hACE2 binding. Journal of Biomolecular Structure & Dynamics: 1–10. PMID33030105. DOI: 10.1080/07391102.2020.1830854.
(augustus 2021). Considerations for the discovery and development of 3-chymotrypsin-like cysteine protease inhibitors targeting SARS-CoV-2 infection. Current Opinion in Virology49: 36–40. PMID34029993. PMC8075814. DOI: 10.1016/j.coviro.2021.04.006.
(september 2021). Rethinking Remdesivir: Synthesis, Antiviral Activity, and Pharmacokinetics of Oral Lipid Prodrugs. Antimicrobial Agents and Chemotherapy65 (10): e0115521. PMID34310217. PMC8448143. DOI: 10.1128/AAC.01155-21.
(augustus 2021). Exploring the Binding Mechanism of PF-07321332 SARS-CoV-2 Protease Inhibitor through Molecular Dynamics and Binding Free Energy Simulations. International Journal of Molecular Sciences22 (17). PMID34502033. PMC8430524. DOI: 10.3390/ijms22179124.
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Ritonavir. The American Society of Health-System Pharmacists. Gearchiveerd op 17 oktober 2015. Geraadpleegd op 23 oktober 2015.
(januari 2004). Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients. The Journal of Antimicrobial Chemotherapy53 (1): 4–9. PMID14657084. DOI: 10.1093/jac/dkh029.
(juni 2001). Ritonavir: an extraordinary example of conformational polymorphism. Pharmaceutical Research18 (6): 859–866. PMID11474792. DOI: 10.1023/A:1011052932607.
(maart 2003). Elucidation of crystal form diversity of the HIV protease inhibitor ritonavir by high-throughput crystallization. Proceedings of the National Academy of Sciences of the United States of America100 (5): 2180–2184. PMID12604798. PMC151315. DOI: 10.1073/pnas.0437744100.
(februari 2017). A Newly Discovered Racemic Compound of Pioglitazone Hydrochloride Is More Stable than the Commercial Conglomerate. Crystal Growth & Design17 (2): 414–417. PMID31537981. PMC6752731. DOI: 10.1021/acs.cgd.6b01638.
(mei 2020). A Trial of Lopinavir-Ritonavir in Adults Hospitalized with Severe Covid-19. The New England Journal of Medicine382 (19): 1787–1799. PMID32187464. PMC7121492. DOI: 10.1056/NEJMoa2001282.
(oktober 2020). Molecular dynamics analysis predicts ritonavir and naloxegol strongly block the SARS-CoV-2 spike protein-hACE2 binding. Journal of Biomolecular Structure & Dynamics: 1–10. PMID33030105. DOI: 10.1080/07391102.2020.1830854.
(augustus 2021). Considerations for the discovery and development of 3-chymotrypsin-like cysteine protease inhibitors targeting SARS-CoV-2 infection. Current Opinion in Virology49: 36–40. PMID34029993. PMC8075814. DOI: 10.1016/j.coviro.2021.04.006.
(september 2021). Rethinking Remdesivir: Synthesis, Antiviral Activity, and Pharmacokinetics of Oral Lipid Prodrugs. Antimicrobial Agents and Chemotherapy65 (10): e0115521. PMID34310217. PMC8448143. DOI: 10.1128/AAC.01155-21.
(augustus 2021). Exploring the Binding Mechanism of PF-07321332 SARS-CoV-2 Protease Inhibitor through Molecular Dynamics and Binding Free Energy Simulations. International Journal of Molecular Sciences22 (17). PMID34502033. PMC8430524. DOI: 10.3390/ijms22179124.