Michael A McDonald1, Kenneth L Watkin. 1. Medical Imaging Research Laboratory, University of Illinois at Urbana-Champaign, Champaign, IL, USA.
Abstract
RATIONALE AND OBJECTIVE: To prepare and characterize new particulate contrast media, small particulate gadolinium oxide (SPGO) and gadolinium oxide albumin microspheres (GOAM), as prototype multimodal imaging and therapeutic agents. METHODS: SPGO was purchased from Alfa Aesar Inc. (Ward Hill, MA). GOAM were synthesized via ultrasonic irradiation using SPGO and 5% bovine serum albumin in aqueous solution. SPGO and GOAM were characterized by size, concentration, structure, and gadolinium content. Their relaxivity at high magnetic field strength and x-ray attenuating abilities were evaluated in 0.4% agar gel at room temperature. RESULTS: SPGO were confirmed to be 20-40 nm in diameter. GOAM have an average size of 2 to 5 microm and show a relatively homogeneous distribution of SPGO within the albumin microspheres. T1 and T2 relaxivity of GOAM was 6.7 seconds(-1) mmol/L(-1) and 38.5 seconds(-1) mmol/L(-1), respectively, while that of SPGO was 0.2 seconds(-1) mmol/L(-1) and 6.8 seconds(-1) mmol/L(-1), respectively. At 0, 0.004, 0.16, 4.0, and 16.0 mmol/L SPGO, x-ray attenuation values were measured at 2.11, 3.48, 7.06, 39.83, and 187.33 Hounsfield units, respectively. CONCLUSIONS: Use of SPGO and SPGO encapsulated in non-heat-hardened albumin microspheres (GOAM) represents a new approach. SPGO and GOAM have suitable physicochemical properties to warrant further biophysical and animal studies and reevaluation of toxicity limitations.
RATIONALE AND OBJECTIVE: To prepare and characterize new particulate contrast media, small particulate gadolinium oxide (SPGO) and gadolinium oxide albumin microspheres (GOAM), as prototype multimodal imaging and therapeutic agents. METHODS: SPGO was purchased from Alfa Aesar Inc. (Ward Hill, MA). GOAM were synthesized via ultrasonic irradiation using SPGO and 5% bovine serum albumin in aqueous solution. SPGO and GOAM were characterized by size, concentration, structure, and gadolinium content. Their relaxivity at high magnetic field strength and x-ray attenuating abilities were evaluated in 0.4% agar gel at room temperature. RESULTS: SPGO were confirmed to be 20-40 nm in diameter. GOAM have an average size of 2 to 5 microm and show a relatively homogeneous distribution of SPGO within the albumin microspheres. T1 and T2 relaxivity of GOAM was 6.7 seconds(-1) mmol/L(-1) and 38.5 seconds(-1) mmol/L(-1), respectively, while that of SPGO was 0.2 seconds(-1) mmol/L(-1) and 6.8 seconds(-1) mmol/L(-1), respectively. At 0, 0.004, 0.16, 4.0, and 16.0 mmol/L SPGO, x-ray attenuation values were measured at 2.11, 3.48, 7.06, 39.83, and 187.33 Hounsfield units, respectively. CONCLUSIONS: Use of SPGO and SPGO encapsulated in non-heat-hardened albumin microspheres (GOAM) represents a new approach. SPGO and GOAM have suitable physicochemical properties to warrant further biophysical and animal studies and reevaluation of toxicity limitations.
Authors: Maria Engström; Anna Klasson; Henrik Pedersen; Cecilia Vahlberg; Per-Olov Käll; Kajsa Uvdal Journal: MAGMA Date: 2006-08-15 Impact factor: 2.310
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