The usage of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.">The usage of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.The usage of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work. usage of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.sage of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.ge of drugs for the treatment and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.and prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.d prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.prevention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.evention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.ention of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.tion of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.of deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work. deseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.eseases starts with their administration into the organism or application onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.cation onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.tion onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.on onto the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.o the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.the body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.e body surface. The route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.he route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work. route of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.oute of administration defines the speed of onset of effect, its intensity and duration. In certain cases the route of administration determines how the medications work.">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).pan class="">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).n class="">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).class="">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).ass="">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract)."">Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).>Existing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).xisting administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).ing administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).g administration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).nistration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).stration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).ration routes are usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).re usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract). usually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).sually subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).lly subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).y subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).subdivided into enteral (via digestive tract) and parenteral (not entering into the digestive tract).igestive tract) and parenteral (not entering into the digestive tract).estive tract) and parenteral (not entering into the digestive tract).tive tract) and parenteral (not entering into the digestive tract).ve tract) and parenteral (not entering into the digestive tract). tract) and parenteral (not entering into the digestive tract).ract) and parenteral (not entering into the digestive tract). and parenteral (not entering into the digestive tract).nd parenteral (not entering into the digestive tract). parenteral (not entering into the digestive tract).ssclass="">Enteral administration comprises oral, sublingual, transbuccal¹, duodenal and rectal routes.ass="">Enteral administration comprises oral, sublingual, transbuccal¹, duodenal and rectal routes.s="">Enteral administration comprises oral, sublingual, transbuccal¹, duodenal and rectal routes.tal routes.l routes.routes.utes.es../span>n>lassss mg src="https://prior.studentlibrary.ru/cgi-bin/mb4x?usr_data=gd-image(doc,ISBN9785970438831-0005,pic_0014.jpg,-1,,00000000,)&hide_Cookie=yes" asis-dx="1062" asis-dy="1526" popup="POPUP-Xz17-pic_0014.jpg;911;1309" onClick="{{;;call_submit('frm_rds','rds','rds|rds','popup_image(doc,ISBN9785970438831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted 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#c0c0c0;cursor:hand;">rds','popup_image(doc,ISBN9785970438831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">s','popup_image(doc,ISBN9785970438831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">,'popup_image(doc,ISBN9785970438831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">38831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">831-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">1-0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">0005,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">05,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">,POPUP-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">P-Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">Xz17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">17-pic_0014.jpg,911,1309)');}return false;}" style="padding:3 3 3 3px;border:1px dotted #c0c0c0;cursor:hand;">px;border:1px dotted #c0c0c0;cursor:hand;">;border:1px dotted #c0c0c0;cursor:hand;">order:1px dotted #c0c0c0;cursor:hand;">1px dotted #c0c0c0;cursor:hand;">x dotted #c0c0c0;cursor:hand;">dotted #c0c0c0;cursor:hand;">rsor:hand;">or:hand;">:hand;">rugs.gs../span>pan>n> class="">¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.lass="">¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.ss="">¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane."">¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.>¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.span>¹ From Latin bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.i>bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.bucca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.cca - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.a - cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.- cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.i>- cheek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.heek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.ek. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.. A number of drugs are taken transbuccally as polymer pastilles. Their active components are absorbed via the oral mucous membrane.heir active components are absorbed via the oral mucous membrane.ir active components are absorbed via the oral mucous membrane. active components are absorbed via the oral mucous membrane.e components are absorbed via the oral mucous membrane.components are absorbed via the oral mucous membrane.mponents are absorbed via the oral mucous membrane.rbed via the oral mucous membrane.ed via the oral mucous membrane. via the oral mucous membrane.pann classs="ter_footr_footlasss="ost common administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.t common administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.common administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.mmon administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.on administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. administration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.nistration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.stration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.ration route is oral (by mouth; internally; per os). This is the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. the most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.he most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. most convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.convenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.nvenient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.enient and simple route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. route of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.oute of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.te of administration. Drugs do not have to be sterile to be administered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.nistered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.stered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.ered this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.ed this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. this way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.his way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.s way. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.y. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply. Absorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.bsorption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. This is a favorable place for absorption due to the large absorbing surface of the intestinal mucous membrane (approximately 200 m²) and its intensive blood supply.ption¹ of a number of substances (for example, acetylsalicylic acid, barbiturates and other weak electrolytes possessing an acidic nature) occurs partially in the stomach² (Fig. II.2). However, the majority of drugs are mainly absorbed in the small intestine. 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The higher the lipophility of substances, the easier they penetrate through the cell membrane.Passive diffusion occurs via the cellular membrane. It is defined by the concentration gradient of the compound. Lipophilic substances (mainly nonpolar) are easily absorbed via this route. The higher the lipophility of substances, the easier they penetrate through the cell membrane.ssive diffusion occurs via the cellular membrane. It is defined by the concentration gradient of the compound. Lipophilic substances (mainly nonpolar) are easily absorbed via this route. The higher the lipophility of substances, the easier they penetrate through the cell membrane.ive diffusion occurs via the cellular membrane. It is defined by the concentration gradient of the compound. Lipophilic substances (mainly nonpolar) are easily absorbed via this route. The higher the lipophility of substances, the easier they penetrate through the cell membrane.e diffusion occurs via the cellular membrane. 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