Evaluation of the Contribution of the Nasal Cavity and Gastrointestinal Tract to Drug Absorption Following Nasal Application to Rats(Biopharmacy)
スポンサーリンク
概要
- 論文の詳細を見る
Drugs applied to the nose in in vivo physiologic condition undergo absorption from the nasal cavity and the gastrointestinal (GI) tract because drug solution in the nasal cavity, together with mucus layer, is cleared to pharynx and then to the GI tract by coordinated beat of the cilia on nasal epithelial cells. The purpose of this study was to develop evaluate the contribution of the nasal cavity and the GI tract to drug absorption following nasal application and to clarify the relation to the transepithelial permeability of the drug (the permeability to Caco-2 monolayer, P_<Caco-2>). Male Wistar rats received intravenous, nasal, and oral drug administration and drug concentration-time profiles in plasma were determined. Fractional absorption after nasal application (F_n) and oral administration (F_<po>) were calculated from the area under the curve following intravenous injection (AUC_<iv>, nasal application (AUC_n), and oral administration (AUC_<po>) as AUC_n/AUC_<iv> and AUC_<po>/AUC_<iv>, respectively. Fractional absorption from the nasal cavity (F_<NC>) and the GI tract (F_<GI>) following nasal application was calculated as (F_n-F_<po>)/(1-F_<po>) and F_<po>(1-F_<NC>), respectively, The shape of the curve between F_<NC> and P_<Caco-2> was similar with the one observed in the case of oral bioavailability except the curve shifted right. It is noteworthy that the relation between F_<GI> and P_<Caco-2> showed a bell-shaped curve with peak at 10^<-6>cm/s of P_<Caco-2>. Highly permeable drug is primarily absorbed through the nasal mucosa before it is cleared to the GI tract. With the decrease in P_<Caco-2>, the larger amount of the drug is cleared to the GI tract and absorption from the GI tract is increased. Poorly permeable drug, on the other hand, was absorbed neither from the nasal was nor the GI tract. These findings suggest that the primary absorption site of drug after nasal application is decided by mucociliary clearance and absorption through the nasal mucosa.
- 公益社団法人日本薬学会の論文
- 2007-03-01
著者
-
Higashi Yutaka
School Of Pharmacy Shujitsu University
-
Yamashita S
Setsunan Univ. Osaka Jpn
-
Yamashita S
Facuty Of Pharmaceutical Sciences Setsunan University
-
FURUBAYASHI Tomoyuki
School of Pharmacy, Shujitsu Universiry
-
KAMAGUCHI Akiko
School of Pharmacy, Shujitsu Universiry
-
KAWAHARADA Kazushi
Facuty of Pharmaceutical Sciences, Setsunan University
-
MASAOKA Yoshie
Facuty of Pharmaceutical Sciences, Setsunan University
-
KATAOKA Makoto
Facuty of Pharmaceutical Sciences, Setsunan University
-
YAMASHITA Shinji
Facuty of Pharmaceutical Sciences, Setsunan University
-
SAKANE Toshiyasu
School of Pharmacy, Shujitsu Universiry
-
Masaoka Yoshie
Facuty Of Pharmaceutical Sciences Setsunan University
-
Kamaguchi Akiko
School Of Pharmacy Shujitsu University
-
Kawaharada Kazushi
Facuty Of Pharmaceutical Sciences Setsunan University
-
Furubayashi Tomoyuki
School Of Pharmacy Shujitsu University
-
Yamashita Shinji
Facuty Of Pharmaceutical Sciences Setsunan University
-
Yamashita S
Fac. Of Pharmaceutical Sciences Setsunan Univ.
-
Sakane Toshiyasu
School Of Pharmacy Shujitsu University
-
Yasui Hiroyuki
Faculty Of Pharmaceutical Science Kyoto University
関連論文
- EVALUATION OF DRUG DISPOSITION IN BRAIN BY MOMENT ANALYSIS (II)
- ELECTROPHYSIOLOGICAL INVERSTIGATIONS ON THE DRUG PERMEATION ACROSS STRATUM CORNEUM (I)
- Effects of Sodium or Glucose Exclusion from the Incubation Medium on Drug Transfer across Rat Jejunal Membrane in Vitro : An Electrophysiological Study(Pharmaceutical)
- EFFECTS OF ABSORPTION PROMOTERS ON THE SELECTIVE PERMEABILITY OF RAT INTESTINAL MEMBRANE TO IONS : ANALYSIS OF PERMEABILITY ENHANCING MECHANISMS BY USING DIFFUSION POTENTIALS
- INVESTIGATIONS OF INFLUX AND ACCUMULATION PROCESSES OF β-LACTAM ANTIBIOTICS AND THEIR ROLE IN THE TRANSMURAL TRANSFER ACROSS RAT JEJUNUM
- FURTHER INVESTIGATIONS ON THE TRANSPORT MECHANISM OF CEPHALEXIN AND AMPICILLIN ACROSS RAT JEJUNUM
- EFFECT OF PHARMACEUTICAL ADJUVANTS ON THE RECTAL PERMEABILITY OF DRUGS
- ELECTROPHYSIOLOGICAL APPROACH TO THE ACTION OF TAURINE ON RAT GASTRIC MUCOSA
- Kinetic Model to Predict the Absorption of Nasally Applied Drugs from in Vitro Transcellular Permeability of Drugs(Biopharmacy)
- Evaluation of the Contribution of the Nasal Cavity and Gastrointestinal Tract to Drug Absorption Following Nasal Application to Rats(Biopharmacy)
- New Methods to Evaluate Intestinal Drug Absorption Mediated by Oligopeptide Transporter from In vitro Study using Caco-2 Cells
- Assessment of Mucosal Immune Response in Genitourinary Tract Using Urine
- Quantitative Evaluation of the Gastrointestinal Absorption of Protein into the Blood and Lymph Circulation
- In Vitro Dissolution/Permeation System to Predict the Oral Absorption of Poorly Water-Soluble Drugs: Effect of Food and Dose Strength on It
- Consideration on Moments of Outflow Profile in Liver Perfusion System with Change in Perfusate Flow Rate Using Oxacillin as Model Drug
- In Vitro Study on the Transport of Zinc across Intestinal Epithelial Cells Using Caco-2 Monolayers and Isolated Rat Intestinal Membranes