Manufacture and characterization of mucoadhesive buccal films

2011 ◽  
Vol 77 (2) ◽  
pp. 187-199 ◽  
Author(s):  
Javier O. Morales ◽  
Jason T. McConville
Keyword(s):  
2020 ◽  
Vol 28 (3) ◽  
pp. 266-273 ◽  
Author(s):  
Gamal M. Zayed ◽  
Saleh Abd-El Rasoul ◽  
Mohamed A. Ibrahim ◽  
Mohammed S. Saddik ◽  
Doaa H. Alshora

Symmetry ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 88
Author(s):  
Maram Diab ◽  
Al-Sayed Sallam ◽  
Imad Hamdan ◽  
Randa Mansour ◽  
Rohanah Hussain ◽  
...  

Insulin mucoadhesive buccal films (MBF) are a noninvasive insulin delivery system that offers an advantageous alternative route of administration to subcutaneous injection. One major concern in the formulation of insulin MBF is the preservation of an insulin secondary structure in the presence of the other film components. Buccal films were formulated using chitosan, glycerin, and L-arginine. The MBF-forming solutions (MBF-FS) and the films (MBF) were examined for their chemical and structural stability and for their in vivo activity. Enzyme-Linked Immunosorbent Assay (ELISA) of the insulin-loaded MBF showed that each individualized unit dose was at least loaded with 80% of the insulin theoretical dose. Results of Synchrotron Radiation Circular Dichroism (SRCD) measurements revealed that MBF-FS retained the α-helices and β–sheets conformations of insulin. Fourier transform infrared (FTIR)-microspectroscopy (FTIR-MS) examination of insulin MBF revealed the protective action of L-arginine on insulin structure by interacting with chitosan and minimizing the formation of an unordered structure and β-strand. A blood glucose-lowering effect of insulin MBF was observed in comparison with subcutaneous (S.C) injection using a rat model. As a result; chitosan-based MBFs were formulated and characterized using SRCD and FTIR-MS techniques. Furthermore, the results of in vivo testing suggested the MBFs as a promising delivery system for insulin.


2019 ◽  
Vol 24 (8) ◽  
pp. 967-974 ◽  
Author(s):  
Nusaiba K. Al-Nemrawi ◽  
Sara S. M. Alsharif ◽  
Karem H. Alzoubi ◽  
Rami Q. Alkhatib

2008 ◽  
Vol 70 (1) ◽  
pp. 43 ◽  
Author(s):  
Mona Semalty ◽  
A Semalty ◽  
G Kumar
Keyword(s):  

2020 ◽  
Vol 10 (4) ◽  
pp. 9-20
Author(s):  
Arjun KL ◽  
Ashok Kumar P ◽  
Manjunath K ◽  
  Suresh V. Kulkarni
Keyword(s):  

2017 ◽  
Vol 173 ◽  
pp. 638-644 ◽  
Author(s):  
Talitha Caldas dos Santos ◽  
Nicoletta Rescignano ◽  
Laurita Boff ◽  
Flávio Henrique Reginatto ◽  
Cláudia Maria Oliveira Simões ◽  
...  

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


Sign in / Sign up

Export Citation Format

Share Document