Computer :softwares (Word,
Excel, Powerpoint, chemdraw...), Internet (web sites creation with HTML
PHP, javascript...),
bioinformatic
(sequences algnment,
genes prediction,
3D structure proteins prediction ).
jLanguages : french (mother tong), working knowledge of English
Education
Since june 2006 : PhD study on the biomolecules vectorization
May 2005 : Diplôme de Recherche Technologique. Equivalent to a six-year
university degree in Biotechnology.
Juin 2003 :Ingénieur en biotechnologie. Equivalent to a five-year university degree
in Biotechnology.
Juin 2001 :Master’s degree in organic chemistry. Speciality synthesis, purification
and analysis of biomolecules
professional experiences
Since 2005 : Research mission in a drug delivery company
- Therapeutical proteins formulation for nasal delivery
- Vaccinating proteins formulation for nasal delivery
- Biomolecules formulation for topical administration
- Peptide formulation for intravenous administration
- Supervisation of preclinic studies in the rabbit
- Chemical synthesis of enhancer for nasal delivery
- stability analysis of formulated proteins by circular dichroïsm
- Formulated proteins hydrodynamic radius determined by light scattering
2002 :Research mission of 6 months in a pharmaceutical company
- Chemical synthesis of IL-8 inhibitor receptors
- multistep synthesis of phenylsulfonamid
- Use of GC for the calculation of endo/exo product proportions generated by a
chemical reaction
- stereoisomer separation by HPLC
- synthesis product control by NMR
2001 :Research mission of 4 months in the LAPP group (UMR 5810)
- chemical synthesis of a tetrapeptide
- Chemical cyclisation of the
tetrapeptide in order to increase its lipophylicity
- purity synthesized peptide determined by HPLC
-
Control of the synthesized peptide by NMR
Publications
C. Bijani, S. Varray, R. Lazaro, J. Martinez, F. Lamaty, N. Kieffer. Cyclic RGD peptide by ring-closing metathesis. Tetrahedron Letters 43 (2002) 3765 – 3767.
A. Aramini,* M. C. Cesta, S. Coniglio, C. Bijani, S. Colagioia, V. D'Elia, and M. Allegretti*. Synthesis of E-Aryl Ethenesulfonamides: A Simple One-Pot, Two-Step Procedure from 1-Hydroxy-1-arylalkanes. J. Org. Chem., 68 (2003), 7911 -7914