• 제목/요약/키워드: Lansoprazole

검색결과 26건 처리시간 0.024초

2-HP-β-시클로덱스트린과 메글루민을 이용한 란소프라졸의 포접화합물 제조 및 평가 (Preparation and Evaluation of Inclusion Complex of Lansoprazole with 2-HP-β-Cyclodextrin and Meglumine)

  • 이정우;김정수;장혜진;이계원;지웅길
    • Journal of Pharmaceutical Investigation
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    • 제34권4호
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    • pp.269-274
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    • 2004

  • To enhance the solubility and stability of lansoprazole (LAN), new proton pump inhibitor, we were prepared various molar ratio of inclusion complex with $2-hydroxypropyl-{\beta}-cyclodextrin$ (HPCD) and organic alkali agent, meglumine (MEG). Inclusion complex formation of LAN with HPCD was investigated by Differential Scanning Calorimetry and X-ray diffractometry. The aqueous solubilities of inclusion complexes, and the stabilities of 1:4 and 1:5 inclusion complexes in aqueous solutions containing different concentrations of MEG were examined. The stability of 1:5 LAN-HPCD inclusion complex containing MEG, which was equaled to amount of LAN, was performed in 0.9% NaCl and 5% dextrose solution. The formation of inclusion complex of LAN with HPCD was $A_L$ type and the molar ratio of complex was 1:1. The stability constant was $41.557\;M^{-1}$. As molar ratio of LAN to HPCD was increased, solubility of inclusion complex was increased. 1:5 LAN-HPCD inclusion complex was more stable than 1:4 LAN-HPCD inclusion complex. And as contained MEG amount in LAN solution was increased, stability of 1:4 and 1:5 LAN-HPCD inclusion complexes was improved. Also stability of 1:5 LAN-HPCD-MEG inclusion complex in 0.9% NaCl solution and 5% dextrose solution was similar to it in water at room temperature, but it was unstable at $40^{\circ}C$.

  • https://doi.org/10.4333/KPS.2004.34.4.269 인용 PDF KSCI

알코올성 위염 동물 모델에서 작두콩 추출물의 보호 효과 (Protective Effect of Canavalia gladiata on Gastric Inflammation Induced by Alcohol Treatment in Rats)

  • 김옥경;남다은;유양희;전우진;이정민
    • 한국식품영양과학회지
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    • 제42권5호
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    • pp.690-696
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    • 2013

  • 본 연구는 국내에서 재배되는 작두콩 추출물의 투여가 알코올 처리로 유발된 위염 동물모델에서 위 점막 손상, 위액분비, 염증성 인자 발현의 변화에 미치는 영향을 관찰한 후 위장 보호 효과의 기능성을 입증시켜 기능성 식품 개발의 기초자료를 제공하고자 하였다. 작두콩 80% 알코올 추출물을 투여한 그룹에서 알코올성 위염을 유발시킨 그룹에 비하여 위 점막 손상과 출혈이 감소하였음을 관찰하였으며 위 손상면적 또한 유의적으로 감소시켰다. 위액분비량을 비교한 결과에서도 알코올성 위염으로 인하여 증가한 위액분비량을 작두콩 80% 알코올 추출물이 농도 의존적으로 감소시켰음을 확인할 수 있었다. 위 조직의 병리학적인 관찰을 통하여 효과를 관찰한 결과 알코올성 위염을 유발한 군에서 위 점막조직의 손상과 표면 상피세포의 손실을 관찰할 수 있었으나, 작두콩 80% 알코올 추출물 250 및 500 mg/kg 투여한 군들에서는 알코올성 위염 그룹과 비교하여 손상이 깊지 않음을 확인할 수 있었다. TBARS 양으로 산화적 손상을 측정한 결과에서는 작두콩 80% 알코올 추출물 500 mg/kg을 투여한 그룹에서 알코올성 위염으로 인하여 증가된 산화적 손상을 대조물질 lansoprazole 30 mg/kg 투여군과 유의적인 차이가 없는 정도로 감소시켰음을 확인하였다. 염증 관련인자인 COX-2와 NF-${\kappa}B$의 발현을 비교한 결과, 알코올성 위염을 유발시킨 시험대조군에서 정상대조군보다 COX-2와 NF-${\kappa}B$의 발현이 확연히 증가한 반면 대조물질 lansoprazole 30 mg/kg 투여한 그룹에서는 발현이 감소하는 것을 확인할 수 있었으나 작두콩 80% 알코올 추출물을 투여한 군에서는 시험대조군에 비해 미비한 감소를 보였다. 따라서 작두콩 80% 알코올 추출물의 알코올성 위염 예방 효과는 형태학적 및 병리학적 관찰, 산화적 손상 억제, 염증억제효과 등으로 확인한 결과, 알코올성 위염을 억제시켰으며 이는 저용량 보다는 고용량을 섭취하였을 때 그 보호효과가 크다는 것을 확인하였다.

  • https://doi.org/10.3746/jkfn.2013.42.5.690 인용 PDF KSCI

0.1% Iodoacetamide에 의해 유도된 흰쥐 위염 모델에서 한약처방(JAUN-1)의 유익한 효능규명 (Beneficial Effects of Herbal Mixture (JAUN-1) on 0.1% Iodoacetamide-induced Gastritis Rat Model)

  • 한경주;구성태;황혜숙;김유성;이지은;고미미;정봉연;최선미
    • 동의생리병리학회지
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    • 제21권6호
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    • pp.1549-1554
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    • 2007

  • To verify the effects of JAUN-1, which is a water-extracted herbal mixture, on gastroenteric disorders induced by 0.1 percent of iodoacetamide (IA) in rats. We divided four groups, $Na{\"{\i}}ve$ + Distilled Water (DW), 0.1% IA + DW, 0.1% IA + Proton pump inhibitor (Lansoprazole, 5 mg/kg) and 0.1% IA + Herbal mixture (JAUN-1, 50mg/kg) and performed following experimental methods to confirm its advantageous effects against ulcerogenic stomach in rats induced by 0.1% IA; cell cytotoxicity, analysis of lesions score, Hematoxylin & Eosin (H&E) stain, RT-PCR for ${\beta}-actin$, COX-1 and COX-2 and evaluation of intestinal prokinetic activity. No cytotoxicity was elucidated at the concentration of 1, 5, 10, 50, 100, $500\;{\mu}g/ml$ and 1mg/ml JAUN-1 through MTT Assay using by human stomach epithelial AGS cells, respectively. In addition, the JAUN-1 treated group and the lansoprazole treated group significantly decreased in lesions score compared to the DW treated group in the gastritis induced rat model, and results of immunohistochemistry by H&E staining showed that histological recovery in Proton Pump Inhibitor (PPI) and JAUN-1 treated groups rather than the DW administrated group. Another outcome was that ${\beta}-actin$ relative COX-2 expression level was significantly promoted in the DW treated group while ${\beta}-actin$ relative COX-1 expression level was no meaningful change in this rat model. Finally, intestinal prokinetic activity was recovered from low level of prokinetic activity due to 0.1% IA induced gastritis to the similar level of Normal group. These results suggested that JAUN-1 may have beneficial effects against 0.1% IA-induced gastritis rat model through decreasing lesions score, histological recovery, ${\beta}-actin$ relative COX-1, 2 expression level and prokinetic activity.

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