(A) Rectal

(B) Oral

(C) Sublingual

(D) Inhalation

(A) Pretty fast absorption 

(B) A drug is exposed to gastric secretion

(C) A drug is exposed more prominent liver metabolism

(D) A drug can be administrated in a variety of doses

(A) Fast onset of effect

(B) Absorption depends on GI tract secretion and motor function (✓)

(C) A drug reaches the blood passing the liver

(D) The sterilization of medicinal forms is obligatory

(A) Sublingual

(B) Oral

(C) Intravenously

(D) Intramuscula

(A) Oral

(B) Transdermal

(C) Rectal (✓)

(D) Intraduodenal

(A) Rheological parameters of blood

(B) Amount of a substance obtained orally and quantity of intakes

(C) Extent of absorption and hepatic first-pass effect 

(D) Glomerular filtration rate

(A) Plasma protein binding degree of substance

(B) Permeability through the brain-blood barrier

(c) Fraction of an uncharged drug reaching the systemic circulation following any route administration 

(D) Amount of a substance in urine relative to the initial doze

(A) Transport of drugs trough a membrane by means of diffusion

(B) Transport without energy consumption

(C) Engulf of drug by a cell membrane with a new vesicle formation

(D) Transport against concentration gradient (✓)

(A) Low ability to penetrate through the cell membrane lipids (✓)

(B) Penetrate through membranes by means of endocytosis

(C) Easy permeation through the blood-brain barrier

(D) High reabsorption in renal tubules

(A) Lipid-soluble

(B) Non-ionized substances

(C) Hydrophobic substances

(D) Hydrophilic substances