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Sempre più spesso vengono presentate ricerche che coniugano la medicina con la fisica quantistica. Il binomio può sembrare bizzarro, ma molti scienziati sono convinti che proprio in esso consisterà il futuro della scienza medica. Tra questi anche alcuni ricercatori dell’Università di Washington, che hanno sviluppato un metodo per controllare l’attività neurale, forse utilizzabile per ...
Gli adenovirus sono responsabili di una lunga serie di infezioni comuni, dal comune raffreddore ad altre malattie infiammatorie come congiuntiviti, polmoniti o cistiti. Si tratta di organismi che la medicina ha imparato a sconfiggere, ma che risultano comunque estremamente resistenti, per via della loro capacità di sopravvivere a lungo al di fuori di un ospite, anche se l’ambiente in cui vi...
Le donne, durante la menopausa, sono soggette a un irrigidimento delle arterie per il quale non è stata finora individuata alcuna strategia terapeutica. Un team di ricercatori americani ha ora scoperto un cofattore che sintetizza una specifica sostanza chimica in grado di migliorare notevolmente la funzione vascolare. Kerrie Moreau, docente di geriatria presso la School of Medicine dell`Universit...
PUBLICATIONS & PATENTS
- Rita De Santis, Anna Maria Anastasi, Angela Pelliccia, Antonio Rosi, Claudio Albertoni, Antonio
Verdoliva, Fiorella Petronzelli, Valeria D’Alessio, Serenella Serani, Carlo Antonio Nuzzolo.
Chemical Linkage to Injected Tissues Is a Distinctive Property of Oxidized Avidin.
6(6):e21075 (2011)
- Verdoliva A., Rivieccio V., Rossi M.
Simplified b-amyloid peptides for safer Alzheimer Vaccines development
Human Vaccines 6(11):936-947 (2010)
- Deban L, Russo RC, Sironi M, Moalli F, Scanziani M, Zambelli V, Cuccovillo I, Bastone A, Gobbi M, Valentino S, Doni A, Garlanda C, Danese S, Salvatori G, Sassano M, Evangelista V, Rossi B, Zenaro E, Constantin G, Laudanna C, Bottazzi B, Mantovani A.
Regulation of leukocyte recruitment by the long pentraxin PTX3.
Nat Immunol. 11(4):328-34 (2010)
- Inforzato A, Baldock C, Jowitt TA, Holmes DF, Lindstedt R, Marcellini M, Rivieccio V, Briggs DC, Kadler KE, Verdoliva A, Bottazzi B, Mantovani A, Salvatori G, Day AJ.
The angiogenic inhibitor long pentraxin PTX3 forms an asymmetric octamer with two binding sites for FGF2.
J. Biol. Chem. 285(23):17681-92 (2010)
- Pratesi A, Bucelli F, Mori I, Chinol M, Verdoliva A, Paganelli G, Rivieccio V, Gariboldi L, Ginanneschi M.
Biotin Derivatives Carrying Two Chelating DOTA Units. Synthesis, in Vitro Evaluation of Biotinidases Resistance, Avidin Binding, and Radiolabeling Tests
J Med Chem. 53 (1), 432-440 (2010)
- Verdoliva A., Bellofiore P., Rivieccio V., Catello S., Colombo M., Albertoni C., Rosi A., Leoni B., Anastasi A.M., De Santis R.
Biochemical and biological characterization of a new oxidized avidin with enhanced tissue binding properties.
J. Biol. Chem. 285(12):9090-9 (2010)
- Caputo R, Dellagreca M, de Paola I, Mastroianni D, Longobardo L.
Novel sulfur and selenium containing bis-alpha-amino acids from 4-hydroxyproline.
Amino Acids 38(1):305-310 (2010)
- Leali D, Bianchi R, Bugatti A, Nicoli S, Mitola S, Ragona L, Tomaselli S, Gallo G, Catello S, Rivieccio V, Zetta L, Presta M
Fibroblast Growth Factor 2-antagonist Activity of a Long-Pentraxin 3-derived Antiangiogenic Pentapeptide
J Cell Mol Med. 14(8):2109-21 (2010)
- Rossi M., Piovesan P., Ghirardi O., Mastroianni D., Bombardi V., Battistini L., Cencioni M.T., Capobianco D., Borsini F., Colombo M., Verdoliva A
Immunogenic, antigenic, fibrillogenic and inflammatory properties of new simplified ß-Amyloid peptides.
Mol Immunol 46: 2524-2532 (2009)
- De Santis R, Albertoni C, Rosi A, Leoni B, Petronzelli F, D'Alessio V, Nucera E, Salvatori G, Paganelli G, Verdoliva A, Carminati P, Nuzzolo CA.
OXavidin for Tissue Targeting Biotinylated Therapeutics
J. Biomed. Biotechnol. 2009: 921434 (2009)
- Basile G, Peticca M, Cusano P, Catello S.
Yeast-secreted Recombinant Extracellular Domain of Human CD105 Antigen is Able to Bind TGF-beta Type II Receptor In Vitro.
Mol Biotechnol. 41(1):26-34 (2009)
- D’Agostino B., Bellofiore P., De Martino T., Punzo C., Rivieccio V., Verdoliva A.
Affinity purification of IgG monoclonal antibodies using the D-PAM synthetic ligand: chromatographic comparison with protein A and thermodynamic investigation of the D-PAM/IgG interaction.
J Immunol Methods 333(1-2): 126-38 (2008)
- Rossi M., Ruvo M., Marasco D., Colombo M., Cassani G., Verdoliva A.
Anti-allergic properties of a new all-D synthetic immunoglobulin-binding peptide
Mol Immunol 45 (1):226-234 (2008)
- Fantò N, Gallo G, Ciacci A, Semproni M, Vignola D, Quaglia M, Bombardi V, Mastroianni D, Zibella MP, Basile G, Sassano M, Ruggiero V, De Santis R, Carminati P.
Design, synthesis, and in vitro activity of peptidomimetic inhibitors of myeloid differentiation factor 88.
J Med Chem. 51(5):1189-202 (2008)
- Inforzato A, Rivieccio V, Morreale AP, Bastone A, Salustri A, Scarchilli L, Verdoliva A, Vincenti S, Gallo G, Chiapparino C, Pacello L, Nucera E, Serlupi-Crescenzi O, Day AJ, Bottazzi B, Mantovani A, De Santis R, Salvatori G.
Structural characterization of PTX3 disulphide bond network and its multimeric status in cumulus matrix organization.
J. Biol. Chem. 283(15):10147-61 (2008)
- Verdoliva A., Rossi M.
IgE-mediated disorders: current therapeutics and new strategies involving synthetic peptides
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry 7 (4), 252-263 (2008)
- Viparelli F, Cassese A, Doti N, Paturzo F, Marasco D, Dathan NA, Monti SM, Basile G, Ungaro P, Sabatella M, Miele C, Teperino R, Consiglio E, Pedone C, Beguinot F, Formisano P, Ruvo M.
Targeting of PED/PEA-15 molecular interaction with phospholipase D1 enhances insulin sensitivity in skeletal muscle cells.
J Biol Chem. 283(31):21769-78 (2008)
- M. Cianfriglia, M. L. Dupuis, A. Molinari, A. Verdoliva, R. Costi, C. M.aria Galluzzo, M. Andreotti, A. Cara, R.Di Santo and L. Palmisano
HIV-1 Integrase Inhibitors Are Substrates for the Multidrug Transporter MDR1-P-glycoprotein
Retrovirology 4, 17-26 (2007)
- V. Rivieccio, A. Esposito, P. Bellofiore, P. Palladino, M. Sassano, M. Colombo, A. Verdoliva
High-level expression and efficient purification of recombinant human long pentraxin PTX3 in Chinese hamster ovary cells
Protein Expression and Purification 51, 49–58 (2007)
- Basile G., Peticca M., Catello S.
Site-specific biotinylation of human myeloid differentiation protein 88 in D. melanogaster Schneider
Molecular Biotechnology 35(3), 253-261 (2007)
- De Santis R, Albertoni C, Petronzelli F, Campo S, D'Alessio V, Rosi A, Anastasi AM, Lindstedt R, Caroni N, Arseni B, Chiodi P, Verdoliva A, Cassani G, Chinol M, Paganelli G, Carminati P.
Low and high tenascin-expressing tumors are efficiently targeted by ST2146 monoclonal antibody
Clin Cancer Res. 12 (7 Pt 1):2191-6 (2006)
- Camozzi M, Rusnati M, Bugatti A, Bottazzi B, Mantovani A, Bastone A, Inforzato A, Vincenti S, Bracci L, Mastroianni D, Presta M.
Identification of an antiangiogenic FGF2-binding site in the N terminus of the soluble pattern recognition receptor PTX3.
J Biol Chem. 281(32):22605-13 (2006)
- P. Bellofiore, F. Petronzelli, T. De Martino, O. Minenkova, V. Bombardi, A. M. Anastasi, R. Lindstedt, F. Felici, R. De Santis, A. Verdoliva
Identification and refinement of a peptide affinity ligand with unique specificity for a monoclonal anti-tenascin-C antibody by screening of a phage display library
J Chromatogr A 1107(1-2):182-91 (2006)
- Petronzelli F., Pelliccia A., Anastasi A.M., D'Alessio V., Albertoni C., Rosi A., Leoni B., De Angelis C., Paganelli G., Palombo G., Dani M., Carminati P. e De Santis R.
Improved tumor targeting by combined use of two antitenascin antibodies
Clin Cancer Res. 11 (19 Pt 2):7137s-7145s (2005)
- Loiarro M, Sette C, Gallo G, Ciacci A, Fantò N, Mastroianni D, Carminati P, Ruggiero V.
Peptide-mediated interference of TIR domain dimerization in MyD88 inhibits interleukin-1-dependent activation of NF-{kappa}B
J Biol Chem. 280(16):15809-14 (2005)
- A Verdoliva, D Marasco, A De Capua, A Saporito, P Bellofiore, V Manfredi, R Fattorusso, C Pedone, M Ruvo
A new ligand for immunoglobulin G subdomains by screening of a synthetic peptide library
Chembiochem 6 (7): 1242-53 (2005)
- De Santis R, Anastasi AM, D'Alessio V, Pelliccia A, Albertoni C, Rosi A, Leoni B, Lindstedt R, Petronzelli F, Dani M, Verdoliva A, Ippolito A, Campanile N, Manfredi V, Esposito A, Cassani G, Chinol M, Paganelli G, Carminati P
Novel antitenascin antibody with increased tumour localisation for Pretargeted Antibody-Guided RadioImmunoTherapy (PAGRIT).
Br. J. Cancer. 88(7):996-1003 (2003)
- Verdoliva A, Pannone F, Rossi M, Catello S, Manfredi V.
Affinity purification of polyclonal antibodies using a new all-D synthetic peptide ligand: comparison with protein A and protein G.
J Immunol Methods 271:77-88 (2002).
- Rossi, M., Manfredi, V., Ruvo, M., Fassina, G., Verdoliva, A
Sequence-simplification and chimeric assembly: new models of peptide antigen modification.
Mol Immunol. 39:443-51 (2002).
- Marino M, Rossi M, Ruvo M, Fassina G
Novel molecular targets for systemic lupus erythematosus
Curr Drug Targets 3(3):223-8 (2002)
- Fassina, G., Ruvo, M., Palombo, G., Verdoliva, A., Marino, M.
Novel ligands for the affinity-chromatographic purification of antibodies.
J. Biochem. Biophys. Methods 49:481-90 (2001)
- De Falco, S., Rivoletto, M.G., Verdoliva, A., Ruvo, M., Rauchi, A., Marino, M., Senatore, S., Cassani, G., Alberti, A., Pontisso, P, Fassina G.
Cloning and expression of a novel hepatitis B virus-binding protein from HepG2 cells.
J Biol Chem. 276:36613-23 (2001)
- Dani M.
Peptide display libraries: design and construction.
J Recept Signal Transduct Res. 21(4):469-88 (2001)
- Dani M.
Biological libraries.
J Recept Signal Transduct Res. 21(4):447-68 (2001)
- De Falco, S., Ruvo, M., Verdoliva, A., Scarallo, A., Raimondo, D., Raucci, A.and Fassina, G.
N-terminal Myristylation of HBV preS1 domain enhances receptor recognition
J Pept Res. 57:390-400 (2001)
- Verdoliva A, Basile G, Fassina G
Affinity purification of immunoglobulins from chicken egg yolk using a new synthetic ligand.
J Chromatogr B Biomed Sci Appl 749(2):233-42 (2000)
- Marino M, Ippolito A, Ruvo M, Scarallo A, Volpe S, Fassina G.
Prevention of experimental autoimmune encephalomyelitis by encephalitogenic epitope sequence simplified derivatives.
Mol Immunol. 37(16):951-60 (2000)
- Marino M, Ruvo M, De Falco S, Fassina G.
Prevention of systemic lupus erythematosus in MRL/lpr mice by administration of an immunoglobulin-binding peptide.
Nat Biotechnol. 18(7):735-9 (2000)
- Fassina G
Protein A mimetic (PAM) affinity chromatography. Immunoglobulins purification
Methods Mol Biol. 147:57-68 (2000)
- Monti MM, Valanzuolo S, Cassani G, Colombo M
Transgenic tomatoes expressing a cucumber mosaic virus satellite RNA: field testing and analysis of satellite RNA spread
J Plant Pathol. 81 (2):113-122 (1999)
- Marino M, Ippolito A, Fassina G.
Inhibition of experimental autoimmune encephalomyelitis in SJL mice by oral administration of retro-inverso derivative of encephalitogenic epitope P87-99.
Eur J Immunol. 29(8):2560-6 (1999)
- Palombo G, Rossi M, Cassani G, Fassina G.
Affinity purification of mouse monoclonal IgE using a protein A mimetic ligand (TG19318) immobilized on solid supports
J Mol Recognit. 11(1-6):247-9 (1998)
- Palombo G, De Falco S, Tortora M, Cassani G, Fassina G.
A synthetic ligand for IgA affinity purification
J Mol Recognit. 11(1-6):243-6 (1998)
- Guerrier L, Flayeux I, Schwarz A, Fassina G, Boschetti E.
IRIS 97: an innovative protein A-peptidomimetic solid phase medium for antibody purification
J Mol Recognit. 11(1-6):107-9 (1998)
- Fassina, G., Verdoliva, A., Palombo, G., Ruvo, M. and Cassani, G.
Immunoglobulins specificity of TG19318: a novel synthetic ligand for antibody affinity purification”.
J. Mol. Recognit. 11:128-133 (1998)
- Marino M, Corti A, Ippolito A, Cassani G, Fassina G.
Effect of bench-scale culture conditions on murine IgG heterogeneity
Biotechnol Bioeng 54(1):17-25 (1997)
- Fassina G, Verdoliva A, Odierna MR, Ruvo M, Cassani G
A protein A mimetic peptide ligand for the affinity purification of antibodies.
J. Mol. Rec. 9: 564-569 (1996)
- Merli S, De Falco S, Verdoliva A, Tortora M, Villain M, Silvi P, Cassani G, Fassina G
An expression system for the single-step production of recombinant human amidated calcitonin
Protein Expr Purif 7(4):347-54 (1996)
- Verdoliva A, Ruvo M, Cassani G, Fassina G
Topological mimicry of cross-reacting enantiomeric peptide antigens
J Biol Chem 270(51): 30422 (1995)
- Verdoliva A, Ruvo M, Villain M, Cassani G, Fassina G
Antigenicity of topochemically related peptides
Biochim Biophys Acta 1253(1):57-62 (1995)
- Verdoliva A, Cassani G, Fassina G
Affinity Purification of Polyclonal Antibodies Using Immobilized Multimeric Peptides
J Chromatogr B Biomed Appl 664(1):175-83 (1995)
- Merli S, Corti A, Cassani G.
Production of soluble tumor necrosis factor receptor type I in Escherichia coli: optimization of the refolding yields by a microtiter dilution assay
Anal Biochem. 230(1):85-91 (1995)
- Fassina G, Cassani G, Gnocchi P, Fornasiero MC, Isetta AM
Inhibition of interleukin-2/p55 receptor subunit interaction by complementary peptides
Arch Biochem Biophys. 318(1):37-45 (1995)
- Corti A, Merli S, Bagnasco L, D'Ambrosio F, Marino M, Cassani G.
Identification of two forms (31-33 and 48 kD) of the urinary soluble p55 tumor necrosis factor receptor that are differentially N- and O-glycosylated.
J Interferon Cytokine Res. 15(2):143-52 (1995).
- Radulescu RT, Bellitti MR, Ruvo M, Cassani G, Fassina G.
Binding of the LXCXE insulin motif to a hexapeptide derived from retinoblastoma protein.
Biochem Biophys Res Commun. 206(1):97-102 (1995)
- Fassina G.
Complementary peptides as recognition molecole
Agents Actions Suppl. 46:109-20 (1995)
PATENTS
| Int. Publ. No: | WO2011012496 | Int. Appl. No: | PCT/EP2010/060469 |
| TITLE | IMPROVED HUMAN LONG PENTRAXIN 3 EXPRESSION SYSTEM AND USES THEREOF |
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| ABSTRACT | The present invention relates to an eukaryotic expression vector comprising a nucleotide sequence encoding for the human long pentraxin PTX3 protein under the control of an effective promoter and a nucleotide sequence encoding for a selectable marker, recombinant human cell able to provide expression of proteins encoded by the vector and method for the production of the human long pentraxin PTX3 protein. |
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| Int. Publ. No: | EP2106802 | Int. Appl. No: | EP20080153968 |
| TITLE | Modified peptides as synthetic vaccines in amyloid-associated disease |
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| ABSTRACT | The present invention relates to new immunogenic peptide derivatives, processes for their preparation, and to pharmaceutical compositions containing the same for the prevention and/or treatment of degenerative diseases, such as Alzheimer's disease. |
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| Int. Publ. No: | WO2009095403 | Int. Appl. No: | PCT/EP2009/050937 |
| TITLE | EXPRESSION SYSTEM AND USES THEREOF FOR THE PRODUCTION OF HUMAN LONG PENTRAXIN 3 |
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| ABSTRACT | The present invention relates to an eukaryotic expression vector comprising a nucleotide sequence encoding for the human long pentraxin PTX3 protein under the control of an effective promoter and a nucleotide sequence encoding for a selectable marker, recombinant human cell able to provide expression of proteins encoded by the vector and method for the production of the human long pentraxin PTX3 protein. |
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| Int. Publ. No: | EP1997826 | Int. Appl. No: | EP20080009793 |
| TITLE | Synthetic ligands for immunoglobulins and pharmaceutical compositions containing them |
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| ABSTRACT | A peptide comprising the sequence of formula: X1 -Arg-Thr-Tyr- (S) where: X1 is the residue of an amino acid, of an amino acid derivative, of a carboxylic acid, or of some other derivative capable of binding covalently to the amino group of arginine, comprising at least one aromatic group. Pharmaceutical composition comprising the aforesaid peptide. Use of the aforesaid peptide for production of a pharmaceutical composition for the treatment of allergic diseases |
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| Int. Publ. No: | US2009/0286726 | Int. Appl. No: | PCT/EP2007/051889 |
| TITLE | USE OF THE LONG PENTRAXIN PTX3 FOR THE PREVENTION OR TREATMENT OF VIRAL DISEASES |
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| ABSTRACT | It is described the use of the long pentraxin PTX3 (PTX3) or one of its functional derivatives, for the preparation of a medicament for the prevention or treatment of viral diseases and /or for inhibiting virus activation |
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| Int. Publ. No: | WO2007085412 | Int. Appl. No: | PCT/EP2007/085412 |
| TITLE | FGF2-BINDING PEPTIDES AND USES THEREOF |
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| ABSTRACT | FGF2-binding peptides are here described, which have been designed starting from the N-terminal region of PTX3, in particular spanning the PTX3(82-110) region. Synthetic peptides related to this sequence are able to bind FGF2 and to inhibit its pro-angiogenic activity in vitro and in vivo with no anticipated impact on innate immunity |
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| Int. Publ. No: | WO2007074496 | Int. Appl. No: | WO2006IT00876 |
| TITLE | Vector for efficient selection and/or maturation of an antibody and uses thereof |
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| ABSTRACT | It is described a vector suitable for efficient selection and/or maturation of a recombinant antibody characterized in that it contains at least one element able to reduce the expression level and/or has an improved efficiency of display of said recombinant antibody |
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| Int. Publ. No: | EP1621546 | Int. Appl. No: | EP20050076751 |
| TITLE | PEPTIDE LIGANDS SPECIFIC TO IMMUNOGLOBULINS |
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| ABSTRACT | A compound of formula: (X1 -X2 -His-X3 -CO)n -R where: X1 is H or an amino acid residue of cysteine (Cys) having L or D configuration, wherein each pair of amino acid residues of Cys, optionally present as X1 , can be in the form of a cystine residue owing to an -S-S- bridge formed by the -SH functions of two Cys residues, X2 is an amino acid residue of tyrosine (Tyr) or of histidine (His) having L or D configuration, X3 is an amino acid residue of Tyr or of His having L or D configuration, provided, however, that X2 is Tyr when X3 is His and X2 is His when X3 is Tyr, His is an amino acid residue of histidine having L or D configuration, n is an integer of from 1 to 4, R when n is 1, is OH, a residue of a single amino acid, or a peptide chain comprising from 2 to 7 amino acids, whereas, when n is 2, 3 or 4, it is a group capable of forming a dimer, a trimer and, respectively, a tetramer. |
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| Int. Publ. No: | WO2005082938 | Int. Appl. No: | PCT/IT2005/000078 |
| TITLE | Anti-human tenascin monoclonal antibody |
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| ABSTRACT | An anti-human tenascin monoclonal antibody is described, whose light and heavy chain variable region sequences are SEQ ID NO: 1 and SEQ ID NO: 2, respectively, its proteolytic fragments capable of binding to an antigenic epitope within the region A(1-4)-D of human tenascin, its recombinant derivatives, its conjugates and its similar functional analogues capable of binding to an antigenic epitope within the A(1-4)-D region of human tenascin. TM KIPO & WIPO 2007 |
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| Int. Publ. No: | US6426401 | Int. Appl. No: | 09/319273 |
| TITLE | Pharmaceutical composition containing an inhibitor of immunoglobulin-receptor interaction |
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| ABSTRACT | The present invention relates to a pharmaceutical composition comprising a biologically effective amount of a peptide of formula (H2N-X1-CO-Thr-NH- X2-CO)n where NH-X1-CO and NH-X2-CO which are different from one another, are residues of tyrosine or arginine, in L or D configuration, where the hydroxy group of threonine and the guanidine moiety of arginine may be protected by a group conventionally used in peptide chemistry for protecting the hydroxy group and the guanidine moiety, respectively, n is 2, 3, or 4,R is a group capable of forming a dimeric, trimeric, or tetrameric peptide, and a pharmaceutically acceptable inert carrier. |
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| Int. Publ. No: | US6222011 | Int. Appl. No: | US19980177595 |
| TITLE | Antigenic peptides |
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| ABSTRACT | An improved antigenic peptide where the amino acid sequence is modified by replacing one or more amino acids with glycine. |
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| Int. Publ. No: | US5880259 | Int. Appl. No: | US670207 |
| TITLE | PEPTIDE USEFUL AS LIGAND |
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| ABSTRACT | A peptide of formula (H2N-X1-Thr-X2-CO)n-R where X1 and X2, different one another, are an amino acid residue of arginine or tyrosine in configuration L or D, wherein the hydroxy group of threonine and tyrosine and the guanidine moiety of arginine may be protected by a compound conventionally used in peptide chemistry for protecting the hydroxy group and the guanidine moiety, respectively, n is 1, 2, 3 or 4, and R, when n is 2, 3 or 4, is a group suitable for forming a dimer, trimer or tetramer, while, when n is 1, R is OH, a single amino acid residue, or a peptide chain comprising up to 7 amino acid residues. |
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| Int. Publ. No: | US5880259 | Int. Appl. No: | US670207 |
| TITLE | PEPTIDE USEFUL AS LIGAND |
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| ABSTRACT | A peptide of formula (H2N-X1-Thr-X2-CO)n-R where X1 and X2, different one another, are an amino acid residue of arginine or tyrosine in configuration L or D, wherein the hydroxy group of threonine and tyrosine and the guanidine moiety of arginine may be protected by a compound conventionally used in peptide chemistry for protecting the hydroxy group and the guanidine moiety, respectively, n is 1, 2, 3 or 4, and R, when n is 2, 3 or 4, is a group suitable for forming a dimer, trimer or tetramer, while, when n is 1, R is OH, a single amino acid residue, or a peptide chain comprising up to 7 amino acid residues. |
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| Int. Publ. No: | US5656491 | Int. Appl. No: | US19940343542 |
| TITLE | Mobile-module plant for the development and the production of biotechnological products on a pilot scale |
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| ABSTRACT | A mobile-module plant for the development and the production of biotechnological products on a pilot scale comprising equipments for the production, separation, purification and finishing of said products and auxiliary equipments, wherein the plant consists of at least two mobile modules suitable for being connected together and integrated one with the other. Each of the mobile modules comprises a movable container. At least one of the movable containers is provided with a preselected own set of said equipments. At least one of the movable containers is aseptic. |
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