A Spray-Dried, Co-Processed Rice Starch as a Multifunctional Excipient for Direct Compression

A new co-processed, rice starch-based excipient (CS) was developed via a spray-drying technique. Native rice starch (RS) was suspended in aqueous solutions of 10%-15% cross-linked carboxymethyl rice starch (CCMS) and 0.5%-6.75% silicon dioxide (in the form of sodium silicate), before spray drying. T...

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Main Authors: Karnkamol Trisopon (Author), Nisit Kittipongpatana (Author), Ornanong Suwannapakul Kittipongpatana (Author)
Format: Book
Published: MDPI AG, 2020-06-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_5d1d64929b8045bda1d1eb28c76ef041
042 |a dc 
100 1 0 |a Karnkamol Trisopon  |e author 
700 1 0 |a Nisit Kittipongpatana  |e author 
700 1 0 |a Ornanong Suwannapakul Kittipongpatana  |e author 
245 0 0 |a A Spray-Dried, Co-Processed Rice Starch as a Multifunctional Excipient for Direct Compression 
260 |b MDPI AG,   |c 2020-06-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics12060518 
500 |a 1999-4923 
520 |a A new co-processed, rice starch-based excipient (CS) was developed via a spray-drying technique. Native rice starch (RS) was suspended in aqueous solutions of 10%-15% cross-linked carboxymethyl rice starch (CCMS) and 0.5%-6.75% silicon dioxide (in the form of sodium silicate), before spray drying. The resulting CSs were obtained as spherical agglomerates, with improved flowability. The compressibility study revealed an improved plastic deformation profile of RS, leading to better compaction and tensile strength. The presence of CCMS also ensured a rapid disintegration of the compressed tablets. CS-CCMS:SiO<sub>2</sub> (10:2.7), prepared with 10% CCMS, 2.7% silicon dioxide, and 40% solid content, was found to exhibit the best characteristics. Compared to the two commercial DC excipients, Prosolv<sup>®</sup> and Tablettose<sup>®</sup>, the flow property of CS-CCMS:SiO<sub>2</sub> (10:2.7) was not significantly different, while the tensile strength was 23%: lower than that of Prosolv<sup>®</sup> but 4 times higher than that of Tablettose<sup>®</sup> at 196 MPa compression force. The disintegration time of CS-CCMS:SiO<sub>2</sub> (10:2.7) tablet (28 s) was practically identical to that of Tablettose<sup>®</sup> tablet (26 s) and far superior to that of Prosolv<sup>®</sup> tablet (>30 min). These results show that CSs could potentially be employed as a multifunctional excipient for the manufacturing of commercial tablets by DC. 
546 |a EN 
690 |a co-processing 
690 |a direct compression excipient 
690 |a rice starch 
690 |a spray drying 
690 |a sodium silicate 
690 |a cross-linked carboxymethyl starch 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 12, Iss 6, p 518 (2020) 
787 0 |n https://www.mdpi.com/1999-4923/12/6/518 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/5d1d64929b8045bda1d1eb28c76ef041  |z Connect to this object online.