Enhancing paracetamol compressibility using the co-drying technique: Impact on tablet release profile from direct compression

Direct compression is the most acceptable and preferred method for manufacturing tablets. However, the poor flow property and lack of the required compressibility of most active ingredients preclude the direct compression technique. Paracetamol is a widely used analgesic drug, usually formulated in...

Full description

Saved in:
Bibliographic Details
Main Authors: Shreya Sham Naik (Author), Sandesh Narayan Somnache (Author), Ajeet Madhukar Godbole (Author), Clecy Fernandes (Author)
Format: Book
Published: German Journal of Pharmaceuticals and Biomaterials, 2024-08-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_c5b4281d4bd54a9f84c0e1468b0d2f4c
042 |a dc 
100 1 0 |a Shreya Sham Naik  |e author 
700 1 0 |a Sandesh Narayan Somnache  |e author 
700 1 0 |a Ajeet Madhukar Godbole  |e author 
700 1 0 |a Clecy Fernandes  |e author 
245 0 0 |a Enhancing paracetamol compressibility using the co-drying technique: Impact on tablet release profile from direct compression 
260 |b German Journal of Pharmaceuticals and Biomaterials,   |c 2024-08-01T00:00:00Z. 
500 |a 10.5530/gjpb.2024.3.7 
500 |a 2750-624X 
500 |a 2750-6258 
520 |a Direct compression is the most acceptable and preferred method for manufacturing tablets. However, the poor flow property and lack of the required compressibility of most active ingredients preclude the direct compression technique. Paracetamol is a widely used analgesic drug, usually formulated in compressed tablet dosage forms. It is a poorly compressible drug with a hefty dose, usually 300 to 500 mg. In addition, Paracetamol exhibits poor flowability and shows the tendency to cap on tableting due to its poor plasticity and compatibility. The present research work developed Paracetamol DC (Directly Compressible) by co-processing with a mixture of Potato starch and Silicon Dioxide in various ratios using co-freezing and co-drying techniques. Paracetamol DC was assessed for multiple pre-compression and post-compression tableting parameters. The marked improvement in flow behavior and compressibility of co-processed Paracetamol was observed. Results of studies showed that Paracetamol DC developed with a 10% mixture containing Potato Starch and Silicon Dioxide in a ratio of 7:3 exhibited better disintegration properties and released more than 50% of the drug within 30 min. The study concluded that the technique of coprocessing poorly compressible drugs such as Paracetamol with starch and  silicon dioxide using the co-freezing co-drying technique could enhance the compressibility and flowability of active pharmaceutical ingredients. 
546 |a EN 
690 |a Poor compressibility 
690 |a co-processing 
690 |a flow ability 
690 |a direct compression 
690 |a paracetamol 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n German Journal of Pharmaceuticals and Biomaterials, Vol 3, Iss 3 (2024) 
787 0 |n https://www.gjpb.de/index.php/gjpb/article/view/118 
787 0 |n https://doaj.org/toc/2750-624X 
787 0 |n https://doaj.org/toc/2750-6258 
856 4 1 |u https://doaj.org/article/c5b4281d4bd54a9f84c0e1468b0d2f4c  |z Connect to this object online.