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The NABIHEAL Project Pioneers Wound Healing with New Biomimetic Matrices

Nearly 40 scientists across 7 countries are pioneering this breakthrough in wound healing using a nobel and affordable bio-inspired, anti-bacterial matrix.

In addition to the vast consortium, the project also comprises 5 small and medium-sized enterprises (SMEs) and 9 academic institutions. These were convened last February at the University of Granada to share insights, progress, and strategies.

According to an article published by UGR at the beginning of this month, about 40 researchers involved in the project have attended a meeting to share results and progress.

The Horizon Europe project NABIHEAL, coordinated by the Biomedical Research Networking Center (CIBER) at the Institute of Materials Science in Barcelona (ICMAB, CSIC), has held a consortium meeting. The international consortium consists of 14 partners from 7 countries, including 5 small and medium-sized enterprises (SMEs) and 9 academic institutions. These partners have expertise in the development, evaluation, and commercialization of products for wound healing, nanotechnology, safety, and regulation.

Who are the NABIHEAL project partners?

There are three groups from CIBER-BBN participating within NABIHEAL: two groups correspond to Unit 6 and Unit 16 of NANBIOSIS. The former is the NANOMOL Group, and is lead by Nora Ventosa, the project coordinator of NABIHEAL. The later corresponds to our Surface Characterization Unit from UEx. The third CIBER-BBN group is the Photonics Engineering Group (GIF) from the University of Cantabria, with several of its leaders working at NABIHEAL.

In addition, researchers from the UGR’s Advanced Therapies: Differentiation, Regeneration, and Cancer group, as well as the Clinical and Translational Dermatology group, are participating as one of the partners in this consortium. Both belong to the ibs.GRANADA Biosanitary Research Institute and the UGR’s Modeling Nature: from nano to macro Excellence Unit.

Professor Juan Antonio Marchal Corrales leads the project at the UGR and is part of the project’s steering and executive committees. This project is developed at the Singular Laboratory of Biofabrication and 3D (bio)printing (BioFabi3D), located at the Biomedical Research Center (CIBM). In addition, UGR and ibs.GRANADA, in collaboration with the company Bioibérica, contribute their expertise in the biofabrication and 3D bio-printing of human skin models based on components of the matrix of each of the skin layers.

About the meeting at UGR:

The meeting, held on February 7th and 8th, was inaugurated by the project coordinator, Nora Ventosa, Scientific Director of Unit 6 of NANBIOSIS and researcher at a researcher at CIBER and ICMAB-CSIC, and by Enrique Herrera, the Vice-Rector for Research and Technology Transfer of the University of Granada.

The meeting was attended by 38 researchers from among the NABIHEAL partners. These included the Biomedical Research Networking Center (CIBER) at the Institute of Materials Science in Barcelona (ICMAB); the University of Extremadura and the University of Cantabria; the Spanish National Research Council (CSIC); Nanomol Technologies S.L. (NT); Bioiberica S.A.U (BIO); Histocell S.L (HCELL); Asphalion (ASPH); MyBiotech GmbH (MyB); Charité-Universitätsmedizin Berlin (CH) from Germany; the Institute for Medical Research and Occupational Health (IMI) from Croatia; the University of Aarhus (AU) from Denmark; the Technion-Israel Institute of Technology (IT) from Israel; BioNanoNet Forschungsgesellschaft mbH (BNN) from Austria, and the University of Maribor (UM) from Slovenia, as reported by the UGR.

About NABIHEAL project:

NABIHEAL, “Nanostructured Antimicrobial Biomaterials for Healing Complex Wounds,” is funded by the Horizon Europe Research and Innovation program. It has a total budget of nearly 5 million EUR for the next four years. The project addresses two unmet medical needs in the healing of complex wounds: firstly, affordable treatments for wound infections and prevention of complications during healing, and secondly, a strategy to optimize the composition and efficacy of drugs and dressings for wound healing.

Aim of the project:

Complex wounds affect the quality of life of more than 2% of the population in developed countries. Thus, it is a global health problem with a significant impact on healthcare economics. Moreover, complex wounds, including chronic wounds or major burns, are highly susceptible to microbial infection and biofilm formation, making them difficult to treat. In this regard, silver is a widely used metal in antimicrobial products for treating wound infections. However, silver-based products are expensive and have various drawbacks due to costs and environmental and safety concerns.

The NABIHEAL project will develop multifunctional biomaterials to address some of the unmet medical needs in wound management. This project will provide affordable treatments for wound infections or prevention of complications during all phases of wound healing.

In the short and medium term, NABIHEAL will develop —at least— two innovative multifunctional biomaterials for wound healing, using affordable manufacturing technologies based in the EU. In the long term, NABIHEAL could become an alternative to silver in wound dressing for wound healing.

You can read more about NABIHEAL project at the official webpage here.

Additional information

The goal of NANBIOSIS is to provide comprehensive and integrated advanced solutions for companies and research institutions in biomedical applications. All of this is done through a single-entry point, involving the design and production of biomaterials, nanomaterials, and their nanoconjugates. This goes along with their characterization from physical-chemical, functional, toxicological, and biological perspectives (preclinical validation).

In order to access our biomedical Solutions, apply here.

NANBIOSIS has worked with pharmaceutical companies of all sizes in the areas of drug delivery, biomaterials and regenerative medicine. Here are a few of them:

Polymeric Micelles Delivering Hope: A Revolutionary Strategy to Fight Cancer

NANBIOSIS researchers reach intracellular targets with encapsulated antibodies.

February 2024, IQAC-CSIC/CIBER-BBN, Barcelona (Spain) and Santiago (Chile)

Dr. Abasolo and her team have developed an innovative strategy to combat intracellular oncogenes, notably KRAS, implicated in various deadly cancers. By encapsulating therapeutic antibodies within polymeric micelles, they have successfully facilitated the entry of these antibodies into cancer cells, targeting internal markers. This breakthrough, achieved through international collaboration, represents a significant advancement in cancer treatment and holds promise for addressing other diseases with intracellular targets. These findings provide hope for improved therapies and outcomes in cancer and beyond.

Every individual is said to have an inner enemy, lurking to sabotage under favorable circumstances. In the case of our cells, this rings particularly true. Some genes are as necessary for their proper function as they are dangerous when they malfunction. Those that, under certain circumstances, promote tumor development are known as oncogenes. But we now have new tools to combat them.

In the ongoing battle against cancer, researchers have reached a significant milestone in combatting intracellular oncogenes. Thanks to a groundbreaking strategy developed by Dr. Abasolo and her team from Unit 20, they managed to reach particularly difficuly intracellular targets. Their innovative approach involves utilizing therapeutic antibodies encapsulated in polymeric micelles, facilitating their entry into cancer cells and targeting internal markers. The results, achieved through international collaboration, mark a significant advancement in cancer treatment and hold promising possibilities for addressing other diseases with intracellular targets.

KRAS is the name given to one of these oncogenes, and it’s a particularly dangerous foe. The small protein produced by the KRAS gene is a molecular switch that controls numerous cellular functions, including survival, proliferation, differentiation, and migration. When KRAS mutates, this switch stops working, preventing the cell from self-regulating, often leading to some of the most malignant and lethal types of cancer, such as pancreatic, colon, or lung cancer. Moreover, this mutated protein is difficult to target due to its unique molecular structure and the fact that it resides within the cell. However, thanks to our new anti-tumor technology, we’re able to reach it.

One method of blocking mutated KRAS is through the use of therapeutic antibodies. These antibodies, by specifically binding to the protein, inhibit its function, halting the malignancy of cancer cells. However, one of the challenges in using these antibodies is that they cannot enter cells on their own. None of the attempts to internalize them have been successful, until now.

In a recent study published last year, the team led by Dr. Abasolo, in which our Unit 20 is integrated, has successfully attacked mutated KRAS using anti-KRAS antibodies. To achieve this, they encapsulated the antibodies in nanometric drug delivery systems (NanoDDS). Specifically, they used micelles composed of a polymer capable of surrounding the antibodies, facilitating their entry into cells. Furthermore, these nanostructures enable passive and selective entry into tumors and, to top it off, the polymer used prevents the emergence of dreaded cancer multi-drug resistances.

These unprecedented results are the product of international collaboration, where in silico simulation, in vitro assays, and animal studies have gone hand in hand. These results have demonstrated the effectiveness of a new tool capable not only of serving in the fight against cancer, but also of acting on therapeutic intracellular targets present in many other diseases. A way to defeat that inner enemy.

References

[1] Diana Rafael, Sara Montero, Pilar Carcavilla, Fernanda Andrade, Júlia German-Cortés, Zamira V. Diaz-Riascos, Joaquin Seras-Franzoso, Monserrat Llaguno, Begoña Fernández, Alfredo Pereira, Esteban F. Duran-Lara, Simó Schwartz Jr., and Ibane Abasolo. Intracellular Delivery of Anti-Kirsten Rat Sarcoma Antibodies Mediated by Polymeric Micelles Exerts Strong In Vitro and In Vivo Anti-Tumorigenic Activity in Kirsten Rat Sarcoma-Mutated Cancers. ACS Applied Materials & Interfaces 2023 15 (8), 10398-10413 DOI: 10.1021/acsami.2c19897

Additional information

In this project, Unit 20 of the NANBIOSIS ICTS has collaborated, providing both functional validation and all preclinical trials with murine models. All of this has been conducted following the strictest ethical guidelines.

The goal of NANBIOSIS is to provide comprehensive and integrated advanced solutions for companies and research institutions in biomedical applications. All of this is done through a single-entry point, involving the design and production of biomaterials, nanomaterials, and their nanoconjugates. This includes their characterization from physical-chemical, functional, toxicological, and biological perspectives (preclinical validation).

In order to access our biomedical Solutions, apply here.

NANBIOSIS has worked with pharmaceutical companies of all sizes in the areas of drug delivery, biomaterials and regenerative medicine. Here are a few of them:

Bringing Hope to Cancer Treatment: New Pioneering Advances in Nanotechnology

NANBIOSIS Researchers Lead the Way in Innovative Nanomedicine Approaches

Cancer remains a formidable challenge globally, with 19.1 million cases diagnosed in 2020, resulting in nearly 10 million deaths. However, amidst these alarming statistics, a beacon of hope emerges from the field of nanomedicine.

Spearheaded by Professor Jesus Santamaria and his team at the NFP group, part of the NANBIOSIS ICTS Unit 9, groundbreaking advancements in nanotechnology are revolutionizing cancer treatment. Funded by the European Research Council, their efforts mark a significant stride towards more effective and targeted therapies.

“The potential adverse effects (of antineoplastic agents) on healthy cells is the main limitation, in addition to the development of drug resistance by cancer cells.”

—Dr. Jose L. Hueso, Scientific Coordinator of Unit 9

Traditional cancer treatments like surgery, chemotherapy (CT), and radiotherapy (RT) have long been the mainstays of clinical intervention. While effective, their indiscriminate nature often leads to debilitating side effects and the development of dreaded drug resistances in cancer cells. Chemotherapy, in particular, poses significant challenges due to its adverse effects on healthy cells.

This is where nanoscience and nanotechnology come to play. These cutting-edge disciplines offer promising avenues for the development of selective and precise cancer therapies. The work of Prof. Santamaria’s team focuses on leveraging nanoparticles to deliver tailored treatments directly to cancerous tissues while minimizing collateral damage to healthy cells.

Their innovative approach involves the synthesis of inorganic and carbon-based nanoparticles with enzyme-mimicking capabilities. These nanoparticles exhibit a multifaceted response within the tumor microenvironment, from consuming glucose to generating reactive oxidative species. Moreover, they disrupt the antioxidant defense mechanisms of cancer cells, rendering them more susceptible to treatment.

Collaborative efforts with esteemed researchers like Pilar Martin Duque, Luisa de Cola, and Asier Unciti-Broceta further enhance the potential of these nanotherapeutic strategies. Together, they strive to refine nanoparticle delivery systems, protect the catalytic activity in the tumor microenvironment, and engineer anticancer prodrugs using bioorthogonal chemistry.

The implications of these advancements are profound. By harnessing the power of nanotechnology, researchers have the tools to revolutionize cancer treatments. With greater specificity and reduced toxicity, nanotherapies offer renewed hope for patients battling this relentless disease.

As the field of nanotechnology continues to evolve, the potential for personalized, precision medicine approaches tailored to individual patients becomes increasingly tangible. With the expertise of NANBIOSIS ICST researchers at the forefront of this revolution, the future of cancer treatment shines brighter than ever before.

Additional information

The goal of NANBIOSIS is to provide comprehensive and integrated advanced solutions for companies and research institutions in biomedical applications. All of this is done through a single-entry point, involving the design and production of biomaterials, nanomaterials, and their nanoconjugates, along with their characterization from physical-chemical, functional, toxicological, and biological perspectives (preclinical validation).

In order to access our biomedical Solutions, apply here.

NANBIOSIS has worked with pharmaceutical companies of all sizes in the areas of drug delivery, biomaterials and regenerative medicine. Here are a few of them:

‘Magic Bullets’ Against Cancer: Unveiling the Potential of DNA Nanoparticles

DNA nanoparticles to selectively target tumor tissues through precise control of the synergies between transported drugs.

February 2024, IQAC-CSIC/CIBER-BBN, Barcelona. The team led by Drs. Carme Fàbrega and Ramón Eritja, in close collaboration with 3 units of the NANBIOSIS ICTS, has developed a new strategy to improve the efficacy and reduce the toxicity of anticancer drugs. They have chemically linked several cytotoxic drugs, currently used in the treatment of various types of tumors, to DNA nanostructures. These structures selectively target cancerous tissues through folate receptors. This tactic allows precise control of drug concentration and exploits their combined effect. The results of this study represent a significant step forward towards the development of more effective and safer cancer treatments. This year 2024, they published their study in the Nanomedicine journal by Elsevier.

“The ‘Magic Bullet’ of Dr. Ehrlich” is not the title of an old pulp magazine. Rather, it is the concept that the German physician and Nobel Prize winner coined to refer to an ideal therapeutic agent capable of acting specifically against a particular disease without affecting healthy cells.

In the case of cancer therapies, we are far from reaching that magic bullet. However, science is bringing us closer to it every day.

Many current anticancer drugs are designed to intercalate into the DNA of cells and alter their function, inducing cell death. One of the most significant problems with these therapies is their adverse effects, as these drugs can also affect non-tumor cells. One way to compensate for this is by combining multiple drugs, creating synergies between them. However, this often greatly hinders both drugs from reaching the target tissue at the appropriate concentrations to exert their synergy.

A strategy to approach the concept coined by the Nobel Prize involves selectively directing drugs towards cancerous tissues and releasing them in a controlled and localized manner. This increases their concentration in the tumor area, reducing the effect on the rest of the organs and tissues.

Thanks to the ability of many drugs to intercalate into DNA, one of the most promising vehicles are DNA nanostructures. These artificially constructed nanocarriers can retain the drug and, due to their enormous versatility, can be designed to selectively target the tumor. Once there, they release the drug in a controlled manner into the cancer cells, ensuring that healthy tissues are not exposed to a toxic concentration of the drug.

However, these DNA nanocarriers face several challenges: low internalization in diseased cells, low selectivity of the target tissues, or limited control over the amount of drug loaded inside and how it binds. Additionally, they only allow the transport of DNA intercalating drugs, limiting the range of applicable therapies.

In a recent study published in the Nanomedicine journal by Elsevier, the team led by Dr. Carme Fàbrega and Dr. Ramón Eritja, in close collaboration with 3 units of the NANBIOSIS ICTS, present a new approach [1]. Through a strategy to control the binding of the drug and its concentration within their DNA nanostructures, they have succeeded in increasing efficacy and reducing toxicity.

Instead of intercalating the drugs as usual, the researchers chemically conjugated each drug to a piece of the puzzle that would later form the nanostructure. They managed this way to precisely attach three anticancer drugs to their vehicles, each of them acting on a different anticancer mechanism and promoting a synergistic effect between them. Additionally, they achieved selective targeting by binding their nanostructures to folate receptors, expressed massively in a wide variety of tumor types.

This pioneering methodology is capable of attaching multiple drugs to DNA nanostructures, each at predetermined concentrations. This represents a leap forward in advancing towards the generation of that effective and harmless magic bullet that Dr. Ehrlich envisioned.

References

[1] Natalia Navarro, Anna Aviñó, Òscar Domènech, Jordi H. Borrell, Ramon Eritja, Carme Fàbrega, Defined covalent attachment of three cancer drugs to DNA origami increases cytotoxicity at nanomolar concentration, Nanomedicine: Nanotechnology, Biology and Medicine, Volume 55, 2024, 102722, ISSN 1549-9634, DOI: 10.1016/j.nano.2023.102722.

Additional information

In this project, three NANBIOSIS units have collaborated: Unit 12, with a characterization and scientific advisory role; Unit 18, providing one of the nanotoxic drugs; and Unit 29, contributing to the synthesis of oligonucleotides.

The goal of NANBIOSIS is to provide comprehensive and integrated advanced solutions for companies and research institutions in biomedical applications. All of this is done through a single-entry point, involving the design and production of biomaterials, nanomaterials, and their nanoconjugates, along with their characterization from physical-chemical, functional, toxicological, and biological perspectives (preclinical validation).

In order to access our biomedical Solutions, apply here.

NANBIOSIS has worked with pharmaceutical companies of all sizes in the areas of drug delivery, biomaterials and regenerative medicine. Here are a few of them: