The lab's foundational contribution — and what brought it global recognition — is the development of decellularized extracellular matrix (dECM)-based bioinks. By stripping tissues (adipose, cartilage, heart, cornea, liver, skin, muscle) of their cellular content while preserving the biochemical milieu of the native matrix, the lab creates tissue-specific inks that provide cells with an optimized microenvironment far superior to synthetic hydrogels.
Building on this, the lab continually innovates in bioprinting processes. The REFRESH platform uses a PEG-gelatin suspension bath for embedded bioprinting of fragile dECM hydrogels with high structural fidelity. Visible-light crosslinkable silk fibroin bioinks, dual-crosslinking strategies, and multi-material extrusion approaches further expand the bioprinting toolkit toward functional, load-bearing tissue constructs.
KEY PUBLICATIONS & BREAKTHROUGHS
Printing three-dimensional tissue analogues with decellularized extracellular matrix bioink
Pati F, Jang J, Ha D-H, et al. · Nat Commun 5:3935 (2014)
REFRESH — Reversible Embedded Bioprinting for Faster Reinforcement and Structuring of dECM Hydrogels
Meenu TS, Bera AK, Ghosh S, et al. · Adv Healthc Mater e04931 (2026)
Formulation of Dermal Tissue Matrix Bioink by a Facile Decellularization Method
Bera AK, Sriya Y, Pati F · Macromol Biosci 22(8), 2200109 (2022)
Shukla P, Bera AK, Yeleswarapu S, Pati F · Macromol Biosci 2400035 (2024)
Corneal blindness affects millions globally, yet donor tissue supply is critically short. The BioFabTE Lab has built a comprehensive programme to address this — from decellularizing human donor corneas to formulate hydrogel bioinks, to 3D-bioprinting anatomically accurate stromal equivalents, to developing injectable hydrogels that prevent post-traumatic scarring and keratoconus progression.
Recent advances include 4D bioprinted self-morphing corneal equivalents using smart hybrid hydrogels, transparent and adhesive corneal patches combining photo-crosslinkable dopamine-conjugated silk fibroin with dECM, and GMP-grade constructs validated in pre-clinical studies for partial keratoplasty — directly supported by large ICMR funding (₹536.5 L).
KEY PUBLICATIONS & BREAKTHROUGHS
Chameettachal S, Venuganti A, Parekh Y, et al. · Acta Biomater 171, 289–307 (2023)
Ghosh A, Bera AK, Adhikari J, et al. · IJBM 306, 141761 (2025)
Ghosh A, Adhikari J, Ghosh S, et al. · Adv Healthc Mater e02721 (2026)
Chameettachal S, Puranik CJ, et al. · ACS Appl Bio Mater 4(9), 7300–7313 (2021)
ORGANS MODELLED
Liver • Kidney • Skin • Tendon • Trachea
KEY PUBLICATIONS & BREAKTHROUGHS
Kiranmai G, Alam A, Chameettachal S, et al. · ACS AMI 16(39), 52008–52022 (2024)
Kiranmai G, Kaki S, Chameettachal S, et al. · Biomater Adv 185, 214885 (2026)
Sasikumar S, Boden A, Chameettachal S, et al. · ACS Appl Bio Mater 5(6), 3023–3037 (2022)
Sasikumar S, Chameettachal S, Kingshott P, Cromer B, Pati F · ACS BSE 8(2), 834–846 (2022)
Sasikumar S, Chameettachal S, et al. · ACS Appl Bio Mater 6(12), 5224–5234 (2024)
FOCUS AREAS
Triple-negative breast cancer • Liver cancer • Drug efficacy testing
Conventional 2D cancer cell cultures fail to replicate the heterogeneous, stromal-rich tumour microenvironment (TME), leading to poor predictability of drug responses in vivo. The lab develops 3D bioprinted tumour models using tissue-derived dECM hydrogels — notably decellularized adipose tissue for breast cancer — that recapitulate structural complexity, paracrine signalling, and drug resistance phenotypes.
These high-throughput platforms enable rapid screening of drug candidates against patient-like 3D tumour architectures. Work is also ongoing on liver cancer organoids, immuno-competent breast cancer models incorporating immune cells, and bioreactor-enabled cancer-stroma co-culture systems, supported by a current SERB project (₹49.5 L).
KEY PUBLICATIONS & BREAKTHROUGHS
Shukla P, Yeleswarapu S, Heinrich M, Prakash J, Pati F · Biofabrication 14(3), 032002 (2022)
Shukla P, Bera AK, Ghosh A, et al. · Biofabrication 16, 035030 (2024)
Ghosh A, Ghosh S, Pati F, Duraiswamy S · Bioprinting e00316 (2023)
MATERIALS RANGE
PCL • Silk fibroin • Bioactive glass • PETG • Hydroxyapatite
For hard and load-bearing tissue applications, the lab engineers composite scaffolds and printable filaments — combining polycaprolactone (PCL), silk fibroin microfibers, bioactive glass, PETG, and magnesium-doped hydroxyapatite — that balance mechanical performance with biological activity. These constructs have been validated in critical-size rabbit calvaria defect models and oral/maxillofacial surgery contexts.
The work on short silk fibre-reinforced PETG composites, PCL-bioactive glass filaments, and 3D-printed personalised craniomaxillofacial implants bridges additive manufacturing with clinical orthopaedics and dental rehabilitation. Gingival stem-cell-integrated PCL-silk scaffolds show particular promise for personalised bone therapy.
KEY PUBLICATIONS & BREAKTHROUGHS
Pati F, Song T-H, Jang J, et al. · Biomaterials 37, 230–241 (2015)
Bojedla SSR, Kattimani V, et al. · Biomed Mater Devices 1–14 (2023)
Bojedla SSR, Yeleswarapu S, et al. · ACS Appl Bio Mater 5(9), 4465–4475 (2022)
Bhatnagar D, Gautam S, et al. · ACS Appl Bio Mater 7(4), 2272–2282 (2024)
EMERGING FRONTIER
Shape-morphing constructs • Vascular engineering • Self-forming tubular structures
The lab is an active contributor to 4D bioprinting — where a 3D-printed construct changes shape or function over time in response to biological or physical stimuli. Self-forming tubular structures fabricated from bi-layer hydrogel bilayers spontaneously roll into vascular conduits upon hydration, mimicking natural vessel formation. Smart hybrid hydrogels that respond to corneal curvature produce self-morphing stromal equivalents.
Supramolecular hydrogels — including folic acid-based and conductive formulations — are being explored for soft electronics, cardiac tissue applications, and peptide-based cartilage scaffolds. The lab's contributions to the international 4D Printing Roadmap underscore its leadership in this emerging discipline.
KEY PUBLICATIONS & BREAKTHROUGHS
Zeenat L, Zolfagharian A, Bera AK, et al. · IJBM 147088 (2025)
Bodaghi M, Wang L, …, Zeenat L, Pati F, …, Zolfagharian A · SMS 33(11), 113501 (2024)
Zeenat L, Zolfagharian A, Sriya Y, et al. · Adv Mater Technol 2300200 (2023)
Sahu I, Verma J, Bera AK, et al. · ACS AMI 16(26), 34141–34155 (2024)