All Stories

  1. Nanoparticles may influence mast cells gene expression profiles without affecting their degranulation function
  2. Redefining LNP composition: phospholipid and sterol-driven modulation of mRNA expression and immune outcomes
  3. Nano(bio)Materials Do Not Affect Macrophage Phenotype—A Study Conducted by the REFINE Project
  4. Nano(bio)materials Do Not Affect Macrophage Phenotype – A Study Conducted by the REFINE Project
  5. In vitro evaluation of physicochemical-dependent effects of polymeric nanoparticles on their cellular uptake and co-localization using pulmonary calu-3 cell lines
  6. Interlaboratory comparison of endotoxin contamination assessment of nanomaterials
  7. Age-differential CD13 and interferon expression in airway epithelia affect SARS-CoV-2 infection - Effects of vitamin D
  8. Umbilical cord mesenchymal stromal cell-derived extracellular vesicles lack the potency to immunomodulate human monocyte-derived macrophages in vitro
  9. Late Breaking Abstract - Age and vitamin D influence airway epithelial cells response to SARS-CoV-2 infection
  10. Intravenous Administration of Human Umbilical Cord Mesenchymal Stromal Cells Leads to an Inflammatory Response in the Lung
  11. Application of KU812 cells for assessing complement activation related effects by nano(bio)materials
  12. Preclinical Evaluation of Long-Acting Emtricitabine Semi-Solid Prodrug Nanoparticle Formulations
  13. Fate of intravenously administered umbilical cord mesenchymal stromal cells and interactions with the host's immune system
  14. Polymer–prodrug conjugates as candidates for degradable, long-acting implants, releasing the water-soluble nucleoside reverse-transcriptase inhibitor emtricitabine
  15. Exposure of the Basophilic Cell Line KU812 to Liposomes Reveals Activation Profiles Associated with Potential Anaphylactic Responses Linked to Physico-Chemical Characteristics
  16. Intravenous administration of human umbilical cord mesenchymal stromal cells leads to an inflammatory response in the lung
  17. An inter-laboratory comparison of an NLRP3 inflammasome activation assay and dendritic cell maturation assay using a nanostructured lipid carrier and a polymeric nanomedicine, as exemplars
  18. Exposure of human immune cells, to the antiretrovirals efavirenz and lopinavir, leads to lower glucose uptake and altered bioenergetic cell profiles through interactions with SLC2A1
  19. Physiologically based pharmacokinetic modeling of intravenously administered nanoformulated substances
  20. PBPK Modelling for Intratumoral Biodistribution of Magnetic Iron Oxide Nanoparticles
  21. Linear and branched polymer prodrugs of the water-soluble nucleoside reverse-transcriptase inhibitor emtricitabine as structural materials for long-acting implants
  22. Drug delivery systems as immunomodulators for therapy of infectious disease: Relevance to COVID-19
  23. Methodological needs in the quality and safety characterisation of nanotechnology-based health products: Priorities for method development and standardisation
  24. Firefly luciferase offers superior performance to AkaLuc for tracking the fate of administered cell therapies
  25. Assessment of changes in autophagic vesicles in human immune cell lines exposed to nano particles
  26. AUTOSTERE: Systematic Search for Scaffold Replacement Opportunities within Structural Databases
  27. Scalable nanoprecipitation of niclosamide and in vivo demonstration of long-acting delivery after intramuscular injection
  28. Scalable nanoprecipitation of niclosamide and in vivo demonstration of long-acting delivery after intramuscular injection
  29. Induction of Cytokines by Nucleic Acid Nanoparticles (NANPs) Depends on the Type of Delivery Carrier
  30. Scalable nanoprecipitation of niclosamide and in vivo demonstration of long-acting delivery after intramuscular injection
  31. Dose prediction for repurposing nitazoxanide in SARS‐CoV‐2 treatment or chemoprophylaxis
  32. In Vitro Determination of the Immunogenic Impact of Nanomaterials on Primary Peripheral Blood Mononuclear Cells
  33. Prioritization of Anti‐SARS‐Cov‐2 Drug Repurposing Opportunities Based on Plasma and Target Site Concentrations Derived from their Established Human Pharmacokinetics
  34. Safety assessment of a new nanoemulsion-based drug-delivery system reveals unexpected, drug-free anticoagulant activity
  35. Dose Prediction for Repurposing Nitazoxanide in SARS-CoV-2 Treatment or Chemoprophylaxis
  36. Dose prediction for repurposing nitazoxanide in SARS-CoV-2 treatment or chemoprophylaxis
  37. Prioritisation of potential anti-SARS-CoV-2 drug repurposing opportunities based on ability to achieve adequate plasma and target site concentrations derived from their established human pharmacokinetics
  38. Critical considerations for targeting colorectal liver metastases with nanotechnology
  39. Immunotoxicity Considerations for Next Generation Cancer Nanomedicines
  40. Bridging communities in the field of nanomedicine
  41. Long-Acting Injectable Statins—Is It Time for a Paradigm Shift?
  42. Overview of the blood compatibility of nanomedicines: A trend analysis of in vitro and in vivo studies
  43. Assessment of interactions of efavirenz solid drug nanoparticles with human immunological and haematological systems
  44. Derivation of CYP3A4 and CYP2B6 degradation rate constants in primary human hepatocytes: A siRNA-silencing-based approach
  45. Incompatibility of chemical protein synthesis inhibitors with accurate measurement of extended protein degradation rates
  46. Advances in nanomedicine drug delivery applications for HIV therapy
  47. Lack of interaction of lopinavir solid drug nanoparticles with cells of the immune system
  48. In vitro characterisation of solid drug nanoparticle compositions of efavirenz in a brain endothelium cell line
  49. Functionalized superparamagnetic iron oxide nanoparticles provide highly efficient iron-labeling in macrophages for magnetic resonance–based detection in vivo
  50. Sound understanding of environmental, health and safety, clinical, and market aspects is imperative to clinical translation of nanomedicines
  51. Efavirenz Is Predicted To Accumulate in Brain Tissue: an In Silico , In Vitro , and In Vivo Investigation
  52. Use of mRNA suppression to estimate CYP3A4 protein degradation rate constant in primary human hepatocytes
  53. Accelerated oral nanomedicine discovery from miniaturized screening to clinical production exemplified by paediatric HIV nanotherapies
  54. Towards a rational design of solid drug nanoparticles with optimised pharmacological properties
  55. Cytotoxic chemotherapy and the evolution of cellular and viral resistance to antiretroviral therapy in HIV- infected individuals with lymphoma
  56. Determining the Relationship between Nanoparticle Characteristics and Immunotoxicity: Key Challenges and Approaches
  57. Toxicity and inflammatory response in Swiss albino mice after intraperitoneal and oral administration of polyurethane nanoparticles
  58. Opportunities and Challenges in Nanotechnology-enabled Antiretroviral Delivery
  59. Flow cytometric analysis of the physical and protein-binding characteristics of solid drug nanoparticle suspensions
  60. Interactions of antiretroviral drugs with the SLC22A1 (OCT1) drug transporter
  61. The Application of Nanotechnology to Drug Delivery in Medicine
  62. Partial mitigation of gold nanoparticle interactions with human lymphocytes by surface functionalization with a ‘mixed matrix’
  63. Rilpivirine Inhibits Drug Transporters ABCB1, SLC22A1, and SLC22A2In Vitro
  64. Antiretroviral Solid Drug Nanoparticles with Enhanced Oral Bioavailability: Production, Characterization, and In Vitro-In Vivo Correlation
  65. Interactions between tenofovir and nevirapine in CD4+ T cells and monocyte-derived macrophages restrict their intracellular accumulation
  66. Research Spotlight: Nanomedicines for HIV therapy
  67. High-throughput nanoprecipitation of the organic antimicrobial triclosan and enhancement of activity against Escherichia coli
  68. Association of ABCC10 polymorphisms with nevirapine plasma concentrations in the German Competence Network for HIV/AIDS
  69. IFN-γ 874A>T Genotype Is Associated With Higher CCR5 Expression in Peripheral Blood Mononuclear Cells From HIV+ Patients
  70. Plasma and Intracellular Pharmacokinetics of Darunavir/Ritonavir Once Daily and Raltegravir Once and Twice Daily in HIV-Infected Individuals
  71. Genetic Variants of ABCC10, a Novel Tenofovir Transporter, Are Associated With Kidney Tubular Dysfunction
  72. The role of cytokines in the regulation of drug disposition: extended functional pleiotropism?
  73. Raltegravir Is a Substrate for SLC22A6: a Putative Mechanism for the Interaction between Raltegravir and Tenofovir
  74. Plasma and Intracellular (Peripheral Blood Mononuclear Cells) Pharmacokinetics of Once-Daily Raltegravir (800 Milligrams) in HIV-Infected Patients
  75. HIV protease inhibitors are substrates for OATP1A2, OATP1B1 and OATP1B3 and lopinavir plasma concentrations are influenced by SLCO1B1 polymorphisms
  76. The impact of cytokines on the expression of drug transporters, cytochrome P450 enzymes and chemokine receptors in human PBMC
  77. Detection of ABCC2, CYP2B6 and CYP3A4 in human peripheral blood mononuclear cells using flow cytometry
  78. Handbook of Immunological Properties of Engineered Nanomaterials