TY - JOUR
T1 - Solid-State Interactions at the Core-Coat Interface
T2 - Physicochemical Characterization of Enteric-Coated Omeprazole Pellets Without a Protective Sub-Coat
AU - Sharma, Vishnu Dutt
AU - Akocak, Suleyman
AU - Ilies, Marc A.
AU - Fassihi, Reza
N1 - Publisher Copyright:
© 2015, American Association of Pharmaceutical Scientists.
PY - 2015/8/25
Y1 - 2015/8/25
N2 - Conventionally, scanning electron or transmission microscopy, Raman and near infrared (NIR) spectroscopy, terahertz, florescence, and nuclear magnetic resonance imaging have been used to characterize functional coating structure. This study highlights the use of fluorescence microscopy to investigate the physicochemical stability and coating integrity of the commercially available enteric-coated omeprazole pellets containing a basic excipient and prepared by extrusion and spheronization or drug layering on the nonpareil seed, immediately followed by enteric coating (i.e., absence of protective sub-coat). The nature of coating interface and the likely development of an in situ interfacial layer after the application of enteric coating solution was examined using HPLC, NMR, differential scanning calorimetry (DSC), and fluorescent imaging methods. Likewise for the characterization of the solid pellet structure via fluorescence microscopy, a new approach based on fracturing technique (to avoid surface contamination) rather than microtome sectioning was used and validated. Analytical data showed that the pellets containing omeprazole remained chemically stable (>99.5% recovered). Control of the microenvironmental pH by the addition of alkalinizing excipient within a core formulation or as part of drug layering on top of nonpareil seed appears to efficiently neutralize the acidic effect of enteric coating dispersion. Fluorescence images further illustrate the absence of any discernable in situ layer formation at the coat-core interface.
AB - Conventionally, scanning electron or transmission microscopy, Raman and near infrared (NIR) spectroscopy, terahertz, florescence, and nuclear magnetic resonance imaging have been used to characterize functional coating structure. This study highlights the use of fluorescence microscopy to investigate the physicochemical stability and coating integrity of the commercially available enteric-coated omeprazole pellets containing a basic excipient and prepared by extrusion and spheronization or drug layering on the nonpareil seed, immediately followed by enteric coating (i.e., absence of protective sub-coat). The nature of coating interface and the likely development of an in situ interfacial layer after the application of enteric coating solution was examined using HPLC, NMR, differential scanning calorimetry (DSC), and fluorescent imaging methods. Likewise for the characterization of the solid pellet structure via fluorescence microscopy, a new approach based on fracturing technique (to avoid surface contamination) rather than microtome sectioning was used and validated. Analytical data showed that the pellets containing omeprazole remained chemically stable (>99.5% recovered). Control of the microenvironmental pH by the addition of alkalinizing excipient within a core formulation or as part of drug layering on top of nonpareil seed appears to efficiently neutralize the acidic effect of enteric coating dispersion. Fluorescence images further illustrate the absence of any discernable in situ layer formation at the coat-core interface.
KW - DSC
KW - HPLC
KW - NMR
KW - alkalinizing excipient
KW - enteric coating
KW - florescence microscopy
KW - functional coating layer(s)
KW - omeprazole stability
UR - http://www.scopus.com/inward/record.url?scp=84937814750&partnerID=8YFLogxK
U2 - 10.1208/s12249-014-0263-z
DO - 10.1208/s12249-014-0263-z
M3 - Article
C2 - 25595125
AN - SCOPUS:84937814750
SN - 1530-9932
VL - 16
SP - 934
EP - 943
JO - AAPS PharmSciTech
JF - AAPS PharmSciTech
IS - 4
ER -