scholarly journals Isolation and Phisicochemical Characterization of Microcristalline Cellulose from Ramie (Boehmeria nivea L. Gaud) Based on Pharmaceutical Grade Quality

Author(s):  
Desy Nawangsari ◽  
Anis Yohana Chaerunisaa ◽  
Marline Abdassah ◽  
Sriwidodo Sriwidodo ◽  
Taofik Rusdiana ◽  
...  

Microcrystalline cellulose is the most used material for medicine, which able to be found in fibrous plants. Microcrystal celluloses are being used as filler or binder in dosage formulas in tablets and capsules. This research aimed to produce microcrystalline cellulose from ramie based on pharmaceutical grade parameters. Research method include hemp fiber preparation, α-cellulose isolation, microcrystalline cellulose production, and microcrystalline cellulose characterization which compare with Avicel® PH 102 . Result shown microcrystalline cellulose yield is 57.26%. The result of physicochemical characterization that can comply the specifications of pharmaceutical grade as a pharmaceutical excipient.  Keywods :  Microcrystalline cellulose, Ramie, physicochemical, pharmaceutical grade.

Author(s):  
Desy Nawangsari ◽  
Anis Yohana Chaerunisaa ◽  
Marline Abdassah ◽  
Sriwidodo Sriwidodo ◽  
Taofik Rusdiana ◽  
...  

Microcrystalline cellulose is the most used material for medicine, which able to be found in fibrous plants. Microcrystal celluloses are being used as filler or binder in dosage formulas in tablets and capsules. This research aimed to produce microcrystalline cellulose from ramie based on pharmaceutical grade parameters. Research method include hemp fiber preparation, α-cellulose isolation, microcrystalline cellulose production, and microcrystalline cellulose characterization which compare with Avicel® PH 102 . Result shown microcrystalline cellulose yield is 57.26%. The result of physicochemical characterization that can comply the specifications of pharmaceutical grade as a pharmaceutical excipient.  Keywods :  Microcrystalline cellulose, Ramie, physicochemical, pharmaceutical grade.


RSC Advances ◽  
2017 ◽  
Vol 7 (71) ◽  
pp. 45145-45155 ◽  
Author(s):  
Shan-Shan Wang ◽  
Yong-He Han ◽  
Yu-Xuan Ye ◽  
Xiao-Xia Shi ◽  
Ping Xiang ◽  
...  

Komagataeibacter sp. W1 produced high-quality BC, the properties and synthesis mechanisms of which were analyzed by SEM, XRD and FTIR, and genome sequencing, respectively.


ACS Omega ◽  
2020 ◽  
Vol 5 (45) ◽  
pp. 29189-29198
Author(s):  
Swati Gupta ◽  
Sumita Kachhwaha ◽  
SL Kothari ◽  
Manoj Kumar Bohra ◽  
Rohit Jain

BioResources ◽  
2016 ◽  
Vol 11 (2) ◽  
Author(s):  
N. A. Sri Aprilia ◽  
Y. Davoudpour ◽  
W. Zulqarnain ◽  
H. P. S. Abdul Khalil ◽  
C. I. Che Mohamad Hazwan ◽  
...  

2013 ◽  
Vol 113 ◽  
pp. 87-89 ◽  
Author(s):  
M.K. Mohamad Haafiz ◽  
Azman Hassan ◽  
Zainoha Zakaria ◽  
I.M. Inuwa ◽  
M.S. Islam

2019 ◽  
Vol 38 (2) ◽  
pp. 385 ◽  
Author(s):  
Marwa M. El-Naggar ◽  
Wael S. I. Abou-Elmagd ◽  
Ashraf Suloma ◽  
Hamza A. El-Shabaka ◽  
Magdy T. Khalil ◽  
...  

Author(s):  
Kumar P ◽  
S Kumar ◽  
A Kumar ◽  
M Chander

The purpose of this study was to prepare and characterize solid dispersions of the antibacterial agent Cefdinir with PEG 4000 and PVP K-30 with a view to improve its dissolution properties. Investigations of the properties of the dispersions were performed using release studies, X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR). The results obtained showed that the rate of dissolution of Cefdinir was considerably improved when formulated in solid dispersions with PVP K-30 and PEG 4000 as compared with pure drug and physical mixtures. The results from XRD studies showed the transition of crystalline nature of drug to amorphous form, while FTIR studies demonstrated the absence of drug-carriers interaction.


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