Molecular Imaging Techniques to Study the Biodistribution of Orally Administered 99mTc-Labelled Naive and Ligand-Tagged Nanoparticles

被引:28
作者
Areses, Paloma [1 ]
Agueeros, Ma Teresa [2 ]
Quincoces, Gemma [1 ]
Collantes, Maria [3 ]
Richter, Jose Angel
Lopez-Sanchez, Luisa Ma [1 ]
Sanchez-Martinez, Maria [1 ]
Irache, Juan M. [2 ]
Penuelas, Ivan [1 ,3 ]
机构
[1] Univ Navarra Clin, Clin Univ Navarra, Dept Nucl Med, Radiopharmacy Unit, Pamplona 31008, Spain
[2] Univ Navarra, Dept Pharmaceut & Pharmaceut Technol, Pamplona 31008, Spain
[3] Ctr Appl Med Res CIMA, Small Anim Imaging Res Unit, Pamplona 31008, Spain
关键词
Nanoparticles; Biodistribution; Cyclodextrins; IN-VIVO; GASTROINTESTINAL-TRACT; CYCLODEXTRINS; VITRO; BIOAVAILABILITY; ISOFLURANE; PARTICLES; DELIVERY; POLYMER;
D O I
10.1007/s11307-010-0456-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: Study by molecular imaging the biodistribution of poly(anhydride) nanoparticles after oral administration. Procedures: Poly (anhydride) nanoparticles (NP) and cyclodextrin-tagged nanoparticles (CD-NP) were radiolabelled with Tc-99m. Radiochemical purity was measured with a double-solvent chromatography system and the absence of undesirable components was confirmed by size and polydispersion measurement of the technetium-labelled nanoparticles by photon correlation spectroscopy. Single photon emission computed tomography (SPECT) fused computed tomography (CT) in vivo molecular imaging was used for biodistribution studies in small animals. Results: SPECT-CT images revealed activity only in the gastrointestinal tract. Thirteen percent of the given dose of CD-NP and 3% of the given dose of conventional NP were found in the stomach at 8 h. Conclusion: No evidence of translocation or distribution out of gastrointestinal tract was found. CD-NP moved significantly more slowly inside the gut than conventional NP, probably due to their physico-chemical structure that allows stronger interactions with the gut mucosa.
引用
收藏
页码:1215 / 1223
页数:9
相关论文
共 20 条
[1]   Combined hydroxypropyl-β-cyclodextrin and poly(anhydride) nanoparticles improve the oral permeability of paclitaxel [J].
Agueeros, M. ;
Ruiz-Gaton, L. ;
Vauthier, C. ;
Bouchemal, K. ;
Espuelas, S. ;
Ponchel, G. ;
Irache, J. M. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 38 (04) :405-413
[2]   Simultaneous quantification of different cyclodextrins and Gantrez by HPLC with evaporative light scattering detection [J].
Agüeros, M ;
Campanero, MA ;
Irache, JM .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2005, 39 (3-4) :495-502
[3]   Increased oral bioavailability of paclitaxel by its encapsulation through complex formation with cyclodextrins in poly(anhydride) nanoparticles [J].
Agueros, M. ;
Zabaleta, V. ;
Espuelas, S. ;
Campanero, M. A. ;
Irache, J. M. .
JOURNAL OF CONTROLLED RELEASE, 2010, 145 (01) :2-8
[4]   Bioadhesive properties and biodistribution of cyclodextrin-poly(anhydride) nanoparticles [J].
Agueros, Maite ;
Areses, Paloma ;
Angel Campanero, Miguel ;
Salman, Hesham ;
Quincoces, Gemma ;
Penuelas, Ivan ;
Manuel Irache, Juan .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 37 (3-4) :231-240
[5]   IN-VITRO AND IN-VIVO EVALUATION OF MUCOADHESIVE MICROSPHERES PREPARED FOR THE GASTROINTESTINAL-TRACT USING POLYGLYCEROL ESTERS OF FATTY-ACIDS AND A POLY(ACRYLIC ACID) DERIVATIVE [J].
AKIYAMA, Y ;
NAGAHARA, N ;
KASHIHARA, T ;
HIRAI, S ;
TOGUCHI, H .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :397-405
[6]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[7]   Influence of the surface characteristics of PVM/MA nanoparticles on their bioadhesive properties [J].
Arbós, P ;
Campanero, MA ;
Arnangoa, MA ;
Renedo, MJ ;
Irache, JM .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (01) :19-30
[8]   Gantrez® AN as a new polymer for the preparation of ligand-nanoparticle conjugates [J].
Arbós, P ;
Wirth, M ;
Arangoa, MA ;
Gabor, F ;
Irache, JM .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (03) :321-330
[9]   Labeling efficiency and biodistribution of Technetium-99m labeled nanoparticles: interference by colloidal tin oxide particles [J].
Banerjee, T ;
Singh, AK ;
Sharma, RK ;
Maitra, AN .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 289 (1-2) :189-195
[10]   Cyclodextrins in targeting -: Application to nanoparticles [J].
Duchêne, D ;
Ponchel, G ;
Wouessidjewe, D .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (01) :29-40