Tuning Peptide-Based Nanofibers for Achieving Selective Doxorubicin Delivery in Triple-Negative Breast Cancer

被引:4
作者
Bellavita, Rosa [1 ]
Piccolo, Marialuisa [1 ]
Leone, Linda [2 ]
Ferraro, Maria Grazia [1 ,3 ]
Dardano, Principia [4 ]
De Stefano, Luca [4 ]
Nastri, Flavia [2 ]
Irace, Carlo [1 ]
Falanga, Annarita [5 ]
Galdiero, Stefania [1 ]
机构
[1] Univ Naples Federico II, Sch Med, Dept Pharm, Naples, Italy
[2] Univ Napoli Federico II, Dept Chem Sci, Naples 80126, Italy
[3] Univ Glasgow, Coll Med Vet & Life Sci, Sch Infect & Immun, Glasgow, Scotland
[4] CNR, Inst Appl Sci & Intelligent Syst, Naples, Italy
[5] Univ Naples Federico II, Dept Agr Sci, Portici, Italy
关键词
self-assembling peptides; triple negative breast cancer; nanofiber; on-demand strategy; doxorubicin; IN-VIVO; NANOPARTICLES; MECHANISM; THERAPY; GH625;
D O I
10.2147/IJN.S453958
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Introduction: The design of delivery tools that efficiently transport drugs into cells remains a major challenge in drug development for most pathological conditions. Triple -negative breast cancer (TNBC) is a very aggressive subtype of breast cancer with poor prognosis and limited effective therapeutic options. Purpose: In TNBC treatment, chemotherapy remains the milestone, and doxorubicin (Dox) represents the first -line systemic treatment; however, its non -selective distribution causes a cascade of side effects. To address these problems, we developed a delivery platform based on the self -assembly of amphiphilic peptides carrying several moieties on their surfaces, aimed at targeting, enhancing penetration, and therapy. Methods: Through a single-step self -assembly process, we used amphiphilic peptides to obtain nanofibers decorated on their surfaces with the selected moieties. The surface of the nanofiber was decorated with a cell -penetrating peptide (gH625), an EGFR-targeting peptide (P22), and Dox bound to the cleavage sequence selectively recognized and cleaved by MMP-9 to obtain on -demand drug release. Detailed physicochemical and cellular analyses were performed. Results: The obtained nanofiber (NF-Dox) had a length of 250 nm and a diameter of 10 nm, and it was stable under dilution, ionic strength, and different pH environments. The biological results showed that the presence of gH625 favored the complete internalization of NF-Dox after 1h in MDA-MB 231 cells, mainly through a translocation mechanism. Interestingly, we observed the absence of toxicity of the carrier (NF) on both healthy cells such as HaCaT and TNBC cancer lines, while a similar antiproliferative effect was observed on TNBC cells after the treatment with the free-Dox at 50 mu M and NF-Dox carrying 7.5 mu M of Dox. Discussion: We envision that this platform is extremely versatile and can be used to efficiently carry and deliver diverse moieties. The knowledge acquired from this study will provide important guidelines for applications in basic research and biomedicine.
引用
收藏
页码:6057 / 6084
页数:28
相关论文
共 67 条
[1]   The paradoxical functions of EGFR during breast cancer progression [J].
Ali, Remah ;
Wendt, Michael K. .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2017, 2
[2]   Molecular Rotors: What Lies Behind the High Sensitivity of the Thioflavin-T Fluorescent Marker [J].
Amdursky, Nadav ;
Erez, Yuval ;
Huppert, Dan .
ACCOUNTS OF CHEMICAL RESEARCH, 2012, 45 (09) :1548-1557
[3]  
Awad K, 2019, Pharm J, V2019, P1
[4]   Neuroprotective Effects of gH625-lipoPACAP in an In Vitro Fluid Dynamic Model of Parkinson's Disease [J].
Barra, Teresa ;
Falanga, Annarita ;
Bellavita, Rosa ;
Pisano, Jessica ;
Laforgia, Vincenza ;
Prisco, Marina ;
Galdiero, Stefania ;
Valiante, Salvatore .
BIOMEDICINES, 2022, 10 (10)
[5]   gH625-liposomes deliver PACAP through a dynamic in vitro model of the blood-brain barrier [J].
Barra, Teresa ;
Falanga, Annarita ;
Bellavita, Rosa ;
Laforgia, Vincenza ;
Prisco, Marina ;
Galdiero, Stefania ;
Valiante, Salvatore .
FRONTIERS IN PHYSIOLOGY, 2022, 13
[6]   Unveiling the mechanism of action of acylated temporin L analogues against multidrug-resistant Candida albicans [J].
Bellavita, Rosa ;
Annarita, Falanga ;
Merlino, Francesco ;
D'Auria, Gabriella ;
Molfetta, Nicola ;
Saviano, Anella ;
Maione, Francesco ;
Galdiero, Umberto ;
Catania, Maria Rosaria ;
Stefania, Galdiero ;
Grieco, Paolo ;
Roscetto, Emanuela ;
Falcigno, Lucia ;
Elisabetta, Buommino .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2023, 38 (01) :36-50
[7]   Novel temporin L antimicrobial peptides: promoting self-assembling by lipidic tags to tackle superbugs [J].
Bellavita, Rosa ;
Falanga, Annarita ;
Buommino, Elisabetta ;
Merlino, Francesco ;
Casciaro, Bruno ;
Cappiello, Floriana ;
Mangoni, Maria Luisa ;
Novellino, Ettore ;
Catania, Maria Rosaria ;
Paolillo, Rossella ;
Grieco, Paolo ;
Galdieroa, Stefania .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2020, 35 (01) :1751-1764
[8]   gH625 Cell-Penetrating Peptide Promotes the Endosomal Escape of Nanovectorized siRNA in a Triple-Negative Breast Cancer Cell Line [J].
Ben Djemaa, Sanaa ;
Herve-Aubert, Katel ;
Lajoie, Laurie ;
Falanga, Annarita ;
Galdiero, Stefania ;
Nedellec, Steven ;
Souce, Martin ;
Munnier, Emilie ;
Chourpa, Igor ;
David, Stephanie ;
Allard-Vannier, Emilie .
BIOMACROMOLECULES, 2019, 20 (08) :3076-3086
[9]   SYNTHETIC LIPIDATION OF PEPTIDES AND AMINO-ACIDS - MONOLAYER STRUCTURE AND PROPERTIES [J].
BERNDT, P ;
FIELDS, GB ;
TIRRELL, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (37) :9515-9522
[10]   Designer Peptide Amphiphiles: Self-Assembly to Applications [J].
Dasgupta, Antara ;
Das, Debapratim .
LANGMUIR, 2019, 35 (33) :10704-10724