Shielding against breast tumor relapse with an autologous chemo-photo-immune active Nano-Micro-Sera based fibrin implant.
null MimansaMohammad Adeel ZafarDinesh Kumar VermaReena DasJaved Naim AgrewalaAsifkhan ShanavasPublished in: Nanoscale (2024)
Local recurrence post-surgery in early-stage triple-negative breast cancer is a major challenge. To control the regrowth of a residual tumor, we have developed an autologous therapeutic hybrid fibrin glue for intra-operative implantation. Using autologous serum proteins as stabilizers, we have optimized high drug-loaded lapatinib-NanoSera (Lap-NS; ∼66% L.C.) and imiquimod-MicroSera (IMQ-MS; ∼92% L.C). Additionally, plasmonic nanosera (PNS) with an ∼67% photothermal conversion efficiency under 980 nm laser irradiation was also developed. While localized monotherapy with either Lap-NS or PNS reduced the tumor regrowth rate, their combination with IMQ-MS amplified the effect of immunogenic cell death with a high level of tumor infiltration by immune cells at the surgical site. The localized combination immunotherapy with a Nano-MicroSera based hybrid fibrin implant showed superior tumor inhibition and survival with significant promise for clinical translation.
Keyphrases
- early stage
- cell death
- platelet rich plasma
- photodynamic therapy
- multiple sclerosis
- drug delivery
- bone marrow
- cancer therapy
- ms ms
- minimally invasive
- emergency department
- stem cells
- squamous cell carcinoma
- randomized controlled trial
- clinical trial
- machine learning
- radiation therapy
- deep learning
- rectal cancer
- drug release