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Singular

Singular

U7-S03. Characterization by SEM

Characterization by SEM

The Scanning Electron Microscopy service of U7 is specialized in the high-resolution imaging of different samples in the bioengineering field. We can investigate surface morphology and topography of biological samples, polymeric structures and tissue, but also of semiconducting materials, inorganic heterostructures, etc. which are commonly related to biomedical devices and/or biomaterials. We provide advice in the preparation of the samples, as well as assistance in their characterization.

Customer benefits

Our SEM service benefits from being part of a bioengineering-specialized research centre, providing wide knowledge in the treatment and imaging of biological samples, devices and biomaterials. We offer custom services, assuring close and direct interaction with the client, to meet conclusive results and high-quality needs.

Target customer

Our target customers are researchers in the field of bioengineering or R&D departments of biotech companies which want to test, characterize, or compare different samples or prototypes.

Additional information

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U6-S11. Specific density of powders (On-site&Remote) OUTSTANDING

Specific density of powders

Volume and density measurement of porous solids and powders.
Fully automated gas pycnometer, for the measurement of volume and density of powders, granular materials, and solid objects. Typical applications include: porous materials such as catalysts and activated carbons, pharmaceuticals and excipients , foods (raw, refined and end products), ceramics and refractory materials, geological samples (soils, rocks, sediments), building materials (concrete, cement), polymers and composites.
The equipment for this purpose is Ultrapyc 1200e Helium Pycnometer (Quantachrome Instruments).

Customer benefits

The equipment provides density measurements of solids and powders for customers who need to characterise this property and add value to their materials.

Target customer

Universities, public research organisations and pharmacological and chemical industries.

Additional information

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U6-S12. Packed (tapped) density (On-site) OUTSTANDING

Packed (tapped) density

Each particle of a solid material has effectively the same true density regardless of size or shape, but more or less geometric space is occupied by the material according to the relative particle-particle cohesion and mechanical interference. That is, the apparent bulk densities of powdered, granular or flaked materials are highly dependent on the manner in which the particles are packed together. Furthermore, handling or vibration of particulate material causes the smaller particles to work their way into the spaces between the larger particles. The geometric space occupied by the powder decreases and its density increases; ultimately no further natural particle packing takes place without the addition of pressure and maximum particle packing is achieved.
The equipment for this purpose is Autotap (Quantachrome Instruments).

Customer benefits

The equipment provides tapped density measurements of powders for customers who need to characterise this property and add value to their materials.

Target customer

Universities, public research organisations and industries.

Additional information

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U6-S03. Design of experiments (DOE SOFTWARE)

Design of experiments (DOE SOFTWARE)

We offer a Software platform and assitance in performing Design of Experiments, a systematic and statistical approach to planning, conducting, and analyzing experiments or tests. It involves strategically manipulating variables to gather relevant and reliable information while minimizing resources and time.

Customer benefits

DOE helps researchers and engineers understand the relationships between factors, identify optimal conditions, and improve processes by optimizing performance and reducing variability.

Target customer

Manufacturing companies and research groups dealing with experimentation.

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U6-S04. Analysis of particle size, concentration and Z-potential of nanoparticles (On-site&Remote) OUTSTANDING

Analysis of particle size, concentration and Z-potential of nanoparticles

Measurement of the particle size distribution, Z-potential and concentration of solid or dispersed materials (suspensions, liposome, vesicles, emulsions).

The equipments for the analysis are the following:

  • Zetasizer Nano & Ultra (Malvern Panalytical)
  • Mastersizer 2000 (Malvern Panalytical)
  • Nanosight NS300 (Malvern Panalytical)

Customer benefits

The equipment provides particle size, concentration and Z-potential measurements for customers who need to characterise these physico-chemical properties and add value to their materials.

Target customer

Universities, hospitals, public research organisations and pharmacological and chemical industries.

References

  • Nanomedicine 2020 24:102136. 10.1016/j.nano.2019.102136.
  • ACS Appl. Mater. Interfaces 2020, 12, 18, 20253–20262 https://doi.org/10.1021/acsami.0c03040
  • Chem. Mater. 2022, 34, 19, 8517–8527 https://doi.org/10.1021/acs.chemmater.2c00384

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U6-S05. Freeze dryer

Freeze dryer

Freeze drying (also known as lyophilization) is a water (or other solvents) removal process typically used to preserve materials, with the goal of extending their shelf life or reducing its weight. Freeze drying works by freezing the material, then reducing the pressure and adding heat to allow the frozen water in the material to change directly to a vapor (sublimation).

Freeze drying occurs in three phases:

  1. Freezing: Freezing can be done in a freezer, a chilled bath (shell freezer) or on a shelf in the freeze dryer. Cooling the material below its triple point ensures that sublimation, rather than melting, will occur. This preserves its physical form.
  2. Primary Drying: Freeze drying’s second phase is primary drying (sublimation), in which the pressure is lowered and heat is added to the material in order for the water to sublimate. About 95% of the water in the material is removed in this phase. Primary drying can be a slow process.
  3. Secondary Drying: Freeze drying’s final phase is secondary drying (adsorption), during which the ionically-bound water molecules are removed. Most materials can be dried to 1-5% residual moisture.

Customer benefits

  • Solvent removal typically used to preserve materials, with the goal of extending their shelf life or reducing its weight.
  • The design of the equipment offers the best performance in the smallest possible space.
  • Equipment suitable for laboratories: compact and easy to install.
  • Technical reliability and excellent performance.
  • Ease of use: touch screen user interface.

Target customer

  • Pharmaceutical industry
  • Food Industry
  • Chemical industry
  • Materials research centers
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U6-S02. High-pressure phase analysis – solubility, emulsification (Remote) OUTSTANDING

High-pressure phase analysis – solubility, emulsification.

This phase equilibria unit is built for the measurement and detection of phase equilibria and phase transitions by optical means.
The mixture of solute and solvent gas is agitated by the magnetic stirrer. Whenever samples are drawn from the top or the bottom connection in the cell, the directly connected counterbalance piston moves towards the centre of the cell, this keeping the pressure in the measuring cell constant even during the sampling operation. No need to add additional solvent gas, which would change mass ratio and temperature and consequently result in a disturbed equilibrium.

Customer benefits

Phase equilibria cell:
• Capacity: 29-55 mL (depending on piston position)
• Operating pressure max.: 200 Bar
• Operating temperature max.: 150 °C

Counterbalance piston to maintain constant pressure during sampling operation
• Optical windows: 2x ø28mm (sapphire)
• Optical path length: 58 mm

Double wall heating jacket for heating with external thermostat.
High-pressure thermocouple type K (inner temperature)

Target customer

  • Pharmaceutical industry
  • Food Industry
  • Chemical industry
  • Materials research centers

References

N-Grimaldi, et al. ACS Nano 2017, 11, 10774-10784

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U6-S01. Use of High-pressure laboratory-scale plant

Use of High-pressure laboratory-scale plant

with 50, 100 and 300 mL reactors for the processing of biomaterials. Processing of cytotoxic compounds when required.

Preparation of soft molecular materials with controlled structure at supramolecular, micro- and nanoscopic level, using one-step methodologies based on green compressed fluids (i.e. compressed and supercritical CO2).Micro- and nanoparticulate single compounds with high supramolecular homogeneity (i.e., pure polymorphic phases, materials with single polymer folding, etc.).

  • Particulate polymeric matrix uniformly loaded with active compounds (therapeutics, cosmetic ingredients, catalyst, pigments, and dyes, etc.)
  • Dispersed systems (suspensions, liposomes, emulsions, vesicles) with narrow particle size distribution and high morphological homogeneity.
  • Porous materials, either crystalline or amorphous, with defined porosity and porous size.

Customer benefits

Lab-scale high pressure systems, based on a 50 mL, a 100 mL and a 300 mL stirred high pressure autoclaves equipped with pumps for the supply of compressed fluids and liquid solutions. The high-pressure systems can also optionally be equipped with several filters, manometers, thermocouples, and back pressure regulators. The maximum operative pressure is 23 MPa and the maximum operative temperature is 200 °C.
The 300 mL system is also equipped with a mass flowmeter, and a data acquisition system.
All the plants have been designed for micro- and nanostructuring molecular and soft materials.

Target customer

  • Pharmaceutical industry
  • Food Industry
  • Chemical industry
  • Materials research centers

References

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U3-S02. Post synthesis peptide modification (On-site&Remote) OUTSTANDING

Post synthesis peptide modification (On-site&Remote) OUTSTANDING

Post-synthesis peptide modification such as:
– Cyclization through a disulphide bridge, amide, ester, thiosester, thioether, or various staple bonds.
– Biotinylation and/or incorporation of various imaging probes at the N-terminus, C-terminus or on some amino acid side chains (Lys, Cys…).
– Convenient peptide derivatisation for further conjugation by introducing a maleimide, succinimidyl, alkyne or azide-containing spacers.
– Peptide conjugation to polymers, proteins, probes and small molecules.
Multivalent peptide presentation molecules.

Customer benefits

  • Extensive experience in the synthesis of cyclic peptides (disulfide bridge, lactam, lactone, thioester, thioether).
  • Extensive experience in the synthesis of stapled peptides
  • Development of several peptide cyclization methods.
  • Extensive experience in the derivatisation of peptides for conjugation and attachment to various types of molecules (nanoparticles, polymers, imaging probes, small molecules).
  • Development of various strategies for the introduction of post-synthesis modifications.
  • Development of conjugation methodology.
  • Development of methodology for the generation of multivalent peptide presentation molecules.

Target customer

  • Research groups (drug delivery, molecular biology, pharmacology, nanotechnology, biotechnology)
  • Companies (biotech and pharma companies).

References

  • Direct Quantitative Immunochemical Analysis of Autoinducer Peptide IV for Diagnosing and Stratifying Staphylococcus aureus Infections. Montagut, Enrique-J.; Acosta, Gerardo; Albericio, Fernando; Royo, Miriam; Godoy-Tena, Gerard; Lacoma, Alicia ; Prat, Cristina ; Salvador, Juan-Pablo; Marco, Maria-Pilar. ACS Infectious Diseases (2022), 8, 645-656.
  • Hierarchical Quatsome-RGD Nanoarchitectonic Surfaces for Enhanced Integrin-Mediated Cell Adhesion. Martinez-Miguel, Marc; Castellote-Borrell, Miquel; Kober, Mariana; Kyvik, Adriana R. ; Tomsen-Melero, Judit ; Vargas-Nadal, Guillem; Munoz, Jose; Pulido, Daniel ; Cristobal-Lecina, Edgar; Passemard, Solene; oyo, Miriam ; Mas-Torrent, Marta ; Veciana, Jaume ; Giannotti, Marina I. ; Guasch, Judith ; Ventosa, Nora ; Ratera, Imma. ACS Applied Materials & Interfaces (2022), 14, 48179-48193.
  • Engineering a Nanostructured Nucleolin-Binding Peptide for Intracellular Drug Delivery in Triple-Negative Breast Cancer Stem Cells. Pesarrodona, Mireia; Sanchez-Garcia, Laura; Seras-Franzoso, Joaquin; Sanchez-Chardi, Alejandro; Balta-Foix, Ricardo; Camara-Sanchez, Patricia; Gener, Petra; Jara, Jose Juan; Pulido, Daniel ; Serna, Naroa; Schwartz, Simo; Royo, Miriam ; Villaverde, Antonio; Abasolo, Ibane ; Vazquez, Esther. ACS Applied Materials & Interfaces (2020), 12, 5381-5388.
  • Synthesis of Stable Cholesteryl-Polyethylene Glycol-Peptide Conjugates with Non-Disperse Polyethylene Glycol Lengths. Cristobal-Lecina, Edgar; Pulido, Daniel; Martin-Malpartida, Pau; Macias, Maria J.; Albericio, Fernando; Royo, Miriam. ACS Omega (2020), 5, 5508-5519.
  • Highly Versatile Polyelectrolyte Complexes for Improving the Enzyme Replacement Therapy of Lysosomal Storage Disorders. Giannotti, Marina I.; Abasolo, Ibane; Oliva, Mireia; Andrade, Fernanda; Garcia-Aranda, Natalia; Melgarejo, Marta; Pulido, Daniel; Corchero, Jose L.; Fernandez, Yolanda; Villaverde, Antonio; Royo, Miriam; Garcia-Parajo, Maria F.; Sanz, Fausto; Schwartz, Simo. ACS Applied Materials & Interfaces (2016), 8(39), 25741-25752.
  • Gated mesoporous silica nanoparticles using a double-role circular peptide for the controlled and target-preferential release of doxorubicin in CXCR4-expressing lymphoma cells. de la Torre, Cristina; Casanova, Isolda; Acosta, Gerardo; Coll, Carmen; Moreno, Maria Jose; Albericio, Fernando; Aznar, Elena; Mangues, Ramon; Royo, Miriam; Sancenon, Felix; Martinez-Manez, Ramon. Advanced Functional Materials (2015), 25, 687-695.
  • Multivalent dendrimers presenting spatially controlled clusters of binding epitopes in thermoresponsive hyaluronan hydrogels. Seelbach, Ryan J.; Fransen, Peter; Peroglio, Marianna; Pulido, Daniel; Lopez-Chicon, Patricia; Duttenhoefer, Fabian ; Sauerbier, Sebastian; Freiman, Thomas; Niemeyer, Philipp; Semino, Carlos; Albericio, Fernando; Alini, Mauro; Royo, Miriam; Mata, Alvaro; Eglin, David. Acta Biomaterialia (2014), 10, 4340-4350
  • Triazene as a powerful tool for solid-phase derivatization of phenylalanine containing peptides: Zygosporamide analogues as a proof of concept. Torres-Garcia, Carolina; Pulido, Daniel; Albericio, Fernando; Royo, Miriam; Nicolas, Ernesto. Journal of Organic Chemistry (2014), 79(23), 11409-11415.

3. Peptides-System for acidolactic cleavage of the peptide resin boundby anhydrous HF
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U3-S01. Synthesis of peptides and characterisation (On-site&Remote) OUTSTANDING

Synthesis of peptides and characterisation (On-site&Remote) OUTSTANDING

Peptide production on various scales from mg (scale: 10 mg, 50 mg and 100 mg) and grams.
Synthesis of peptides containing phosphorylated amino acids, acylated or methylated side chains (lysine) or non-natural amino acids.
Peptides can be delivered as synthesis crudes (without purification) and purified (≥95% by HPLC).
Peptides are characterized by HPLC and HPLC-MS

Customer benefits

  • Extensive experience on peptide synthesis.
  • Experience in difficult sequences.
  • Control quality at different synthesis points.
  • Capability to design diverse synthesis strategies and purification
  • Development of peptide synthesis methodology.

Target customer

  • Research groups (drug delivery, molecular biology, pharmacology, nanotechnology, biotechnology)
  • Companies (biotech and pharma companies).

References

  • Pharmacological activation of insulin-degrading enzyme improves insulin secretion and glucose tolerance in diet-induced obese mice. Sanz-Gonzalez, Alba; Cozar-Castellano, Irene; Broca, Christophe ; Sabatier, Julia; Acosta, Gerardo A. ; Royo, Miriam ; Hernando-Munoz, Carla; Torroba, Tomas ; Perdomo, German ; Merino, Beatriz. Diabetes, Obesity and Metabolism (2023), 25, 3268-3278.
  • Amide Formation: Choosing the Safer Carbodiimide in Combination with OxymaPure to Avoid HCN Release. Manne, Srinivasa Rao; Luna, Omar; Acosta, Gerardo A.; Royo, Miriam ; El-Faham, Ayman ; Orosz, Gyorgy; de la Torre, Beatriz G. ; Albericio, Fernando. Organic Letters (2021), 23, 6900-6904.
  • Carbosilane Dendron-Peptide Nanoconjugates as Antimicrobial Agents
  • By: Fernandez, Jael; Acosta, Gerardo; Pulido, Daniel; Maly, Marek; Copa-Patino, Jose L.; Soliveri, Juan; Royo, Miriam; Gomez, Rafael; Albericio, Fernando; Ortega, Paula; de la Mata, F. Javier. Molecular Pharmaceutics (2019), 16, 2661-2674.
  • Optimized Stepwise Synthesis of the API Liraglutide Using BAL Resin and Pseudoprolines. Carbajo, Daniel; El-Faham, Ayman; Royo, Miriam; Albericio, Fernando. ACS Omega (2019), 4, 8674-8680
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