Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 72 checked references that resolve
resolves10.1007/s13181-019-00750-xNational Institutes of Health (NIH) Executive Meeting Summary: Developing Medical Countermeasures to Rescue Opioid-Induced Respiratory Depression (a Trans-Agency Scientific Meeting)—August 6/7, 2019
resolves10.1124/jpet.118.256115Fighting Fire with Fire: Development of Intranasal Nalmefene to Treat Synthetic Opioid Overdose
resolves10.1038/clpt.1986.9Nalmefene: Intravenous safety and kinetics of a new opioid antagonist
resolves10.1093/bja/85.4.533Comparison of alfentanil, fentanyl and sufentanil for total intravenous anaesthesia with propofol in patients undergoing coronary artery bypass surgery†
resolves10.1002/jcph.1384Enhanced Intranasal Absorption of Naltrexone by Dodecyl Maltopyranoside: Implications for the Treatment of Opioid Overdose
resolves10.1016/j.brainres.2005.07.060Comparison of the antinociceptive effect of acute morphine in female and male Sprague–Dawley rats using the long-lasting mu-antagonist methocinnamox
resolves10.1124/jpet.119.260331Methocinnamox Produces Long-Lasting Antagonism of the Behavioral Effects of µ-Opioid Receptor Agonists but Not Prolonged Precipitated Withdrawal in Rats
resolves10.1124/jpet.118.253286Reversal and Prevention of the Respiratory-Depressant Effects of Heroin by the Novel μ-Opioid Receptor Antagonist Methocinnamox in Rhesus Monkeys
resolves10.1124/jpet.118.252353Long-Lasting Effects of Methocinnamox on Opioid Self-Administration in Rhesus Monkeys
resolves10.1038/s41386-020-0698-8Effects of acute and repeated treatment with methocinnamox, a mu opioid receptor antagonist, on fentanyl self-administration in rhesus monkeys
resolves10.1007/s00213-020-05592-yMethocinnamox (MCAM) antagonizes the behavioral suppressant effects of morphine without impairing delayed matching-to-sample accuracy in rhesus monkeys
resolves10.1093/jat/21.2.105Plasma Concentrations of Heroin and Morphine-Related Metabolites after Intranasal and Intramuscular Administration
resolves10.1002/phar.2117The Pharmacokinetics and Pharmacodynamics of Carfentanil After Recreational Exposure: A Case Report
resolves10.1136/bmj.2.5919.589Degree and Duration of Reversal by Naloxone of Effects of Morphine in Conscious Subjects
resolves10.1016/S0168-3659(02)00127-XResidual polyvinyl alcohol associated with poly (d,l-lactide-co-glycolide) nanoparticles affects their physical properties and cellular uptake
resolves10.1016/S0168-3659(98)00121-7Lidocaine-loaded biodegradable nanospheres. I. Optimization of the drug incorporation into the polymer matrix
resolves10.1016/S0168-3659(00)00268-6Evaluation of poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO–PPO–PEO) gels as a release vehicle for percutaneous fentanyl
resolves10.1152/japplphysiol.01270.2009The role of medullary serotonin (5-HT) neurons in respiratory control: contributions to eupneic ventilation, CO<sub>2</sub>chemoreception, and thermoregulation
resolves10.1111/j.1469-7793.1998.245bo.xBlockade of synaptic inhibition within the pre‐Bötzinger complex in the cat suppresses respiratory rhythm generation <i>in vivo</i>
resolves10.1016/j.resp.2016.01.007Blockade of dorsolateral pontine 5HT1A receptors destabilizes the respiratory rhythm in C57BL6/J wild-type mice
resolves10.1097/ALN.00000000000004905-HT1A Receptor Agonist Befiradol Reduces Fentanyl-induced Respiratory Depression, Analgesia, and Sedation in Rats
resolves10.1213/ANE.0b013e3181eac011Repinotan, a Selective 5-HT1A-R-Agonist, Antagonizes Morphine-Induced Ventilatory Depression in Anesthetized Rats
resolves10.1038/sj.clpt.6100018The Partial 5-Hydroxytryptamine1A Receptor Agonist Buspirone does not Antagonize Morphine-induced Respiratory Depression in Humans
resolves10.1211/jpp.61.05.0017Brain targeting studies on buspirone hydrochloride after intranasal administration of mucoadhesive formulation in rats
resolves10.1021/acs.jpcb.5b12333Solution-State Structure and Affinities of Cyclodextrin:Fentanyl Complexes by Nuclear Magnetic Resonance Spectroscopy and Molecular Dynamics Simulation
resolves10.1021/acs.jpcb.7b02914Predicting a Drug’s Membrane Permeability: A Computational Model Validated With <i>in Vitro</i> Permeability Assay Data
resolves10.1002/mrc.3803NMR spectroscopic investigation of inclusion complexes between cyclodextrins and the neurotoxin tetramethylenedisulfotetramine
resolves10.1016/j.ejps.2009.07.010Involvement of PI3K-Akt-Bad pathway in apoptosis induced by 2,6-di-O-methyl-β-cyclodextrin, not 2,6-di-O-methyl-α-cyclodextrin, through cholesterol depletion from lipid rafts on plasma membranes in cells
resolves10.1371/journal.pone.0217371Comprehensive molecular pharmacology screening reveals potential new receptor interactions for clinically relevant opioids
resolves10.1136/bcr.05.2010.2986‘I saved a life’: a heroin addict's reflections on managing an overdose using ‘take home naloxone’
resolves10.1016/j.cell.2020.02.052SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor
resolves10.1371/journal.pone.0184876Safety and efficacy of an oxycodone vaccine: Addressing some of the unique considerations posed by opioid abuse
resolves10.4049/jimmunol.1500385The Frequency of Naive and Early-Activated Hapten-Specific B Cell Subsets Dictates the Efficacy of a Therapeutic Vaccine against Prescription Opioid Abuse
resolves10.7326/M20-1210When Epidemics Collide: Coronavirus Disease 2019 (COVID-19) and the Opioid Crisis
resolves10.1016/j.drugalcdep.2019.02.031Overdose following initiation of naltrexone and buprenorphine medication treatment for opioid use disorder in a United States commercially insured cohort
The 15 references without a DOI — listed, not checked
no DOI — not checkedCenters for Disease Control and Prevention (CDC).Vital statistic rapid release: Provisional drug overdose death counts<https://www.cdc.gov/nchs/nvss/vsrr/drug‐overdose‐data.htm> (2020) Accessed August 17 2020.
no DOI — not checkedMethocinnamox is a potent, long‐lasting, and selective antagonist of morphine‐mediated antinociception in the mouse: comparison with clocinnamox, β‐funaltrexamine, and β‐chlornaltrexamine
no DOI — not checkedMu antagonist and kappa agonist properties of beta‐funaltrexamine (beta‐FNA) in vivo: long‐lasting spinal analgesia in mice
no DOI — not checkedIn vivo determination of mu opioid receptor turning in rhesus monkeys after irreversible blockade with clocinnamox
no DOI — not checkedEffects of beta‐funaltrexamine in normal and morphine‐dependent monkeys: observational studies
no DOI — not checkede_1_2_13_33_1
no DOI — not checkedSlow‐sustained delivery of naloxone reduces typical naloxone‐induced precipitated opioid withdrawal effects in male morphine‐dependent mice
no DOI — not checkedReversal of morphine‐induced apnea in the anesthetized rat by drugs that activate 5‐hydroxytryptamine(1A) receptors
no DOI — not checkedAnimal models of nociception
no DOI — not checkedDrug Enforcement Administration Counterfeit Prescription Pills Containing Fentanyls: A Global Threat
no DOI — not checkedVaccination reduces fentanyl distribution to the brain and fentanyl‐induced toxicity in mice and rats: a potential role for a prophylactic vaccine against fentanyl‐induced overdose
no DOI — not checkedCombining a candidate vaccine for opioid use disorders with extended‐release naltrexone increases protection against oxycodone‐induced behavioral effects and toxicity
no DOI — not checkedFormulation and characterization of conjugate vaccines to reduce opioid use disorders suitable for pharmaceutical manufacturing and clinical evaluation
no DOI — not checkedMonoclonal antibodies counteract opioid‐induced behavioral and toxic effects in mice and rats
no DOI — not checkedCenters for Disease Control and Prevention (CDC).CDC Wonder<https://wonder.cdc.gov/> (2020). Accessed July 2 2020
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