Quick definitions for the most commonly misunderstood terms in cell culture, DMPK transporter assays and bioprocessing — written for researchers, DMPK scientists and procurement teams.

Cell Culture & Serum

Term One-line definition Full guide
FBS (Fetal Bovine Serum) The most widely used cell culture supplement — blood serum collected from bovine fetuses, providing growth factors, albumin and nutrients to support cell growth. Read →
Heat Inactivated FBS FBS heated to 56°C for 30 minutes to destroy complement proteins — used in embryo culture, PBMC assays and virus neutralisation. Read →
Low Endotoxin FBS FBS tested to <1 EU/mL endotoxin — required for drug screening, AAV production and cytokine assays where LPS would confound results. Read →
Human Platelet Lysate (hPL) A xeno-free, human-derived FBS alternative produced by freeze-thaw lysis of platelets — releasing concentrated PDGF, EGF, TGF-β and IGF-1 for MSC and primary cell culture. Read →
Off-the-Clot (OTC) Serum Human serum produced by natural clotting — platelets fully activate and release growth factors, giving higher PDGF and EGF than standard plasma-derived serum. Read →

Serum-Free & Albumin

Term One-line definition Full guide
Xeno-Free Cell Culture Cell culture containing no components from a species other than the one being cultured — for human cells, no bovine or murine materials; human-derived supplements (hPL, rHSA) are acceptable. Read →
rHSA (Recombinant Human Serum Albumin) Human serum albumin produced recombinantly in rice or yeast — animal-free, xeno-free, GMP-compatible carrier protein for serum-free cell culture and AAV production media. Read →
Recombinant Human Transferrin (OsrhTF) Animal-free iron delivery protein for serum-free medium — replaces the transferrin function of FBS; essential to prevent iron starvation during serum-free adaptation. Read →

DMPK & Drug Transporters

Term One-line definition Full guide
BSEP (Bile Salt Export Pump) The primary hepatocyte canalicular transporter for bile salt secretion — BSEP inhibition causes intracellular bile salt accumulation and is the leading mechanism of cholestatic drug-induced liver injury (DILI). Read →
P-glycoprotein (P-gp / MDR1 / ABCB1) An ABC efflux transporter expressed at the intestinal epithelium, blood-brain barrier and liver — limits oral bioavailability and CNS penetration; mandatory DDI testing for all NMEs under FDA, EMA and ICH M12. Read →
Vesicular Transport Assay An in vitro method using inside-out membrane vesicles to measure ABC transporter substrate accumulation and inhibitor IC50 — the only viable method for BSEP, MRP2, MRP3, MRP4 where no cell monolayer model exists. Read →
DILI (Drug-Induced Liver Injury) Hepatotoxicity caused by a drug or supplement — the leading cause of post-marketing drug withdrawal. BSEP inhibition is the primary mechanism of cholestatic DILI. Read →

Related Guides


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