In vivo evaluation of antitumoral and antiangiogenic effect of imiquimod-oaded polymeric nanoparticles

被引:37
作者
Dias, Marina Franca [1 ]
Pinheiro de Figueiredo, Bruna Caroline [3 ]
Teixeira-Neto, Julia [3 ]
Andrade Guerra, Maria Carolina [1 ,3 ]
Fialho, Silvia Ligorio [3 ]
Cunha, Armando Silva [2 ]
机构
[1] Univ Fed Goias, Fac Pharm, Goiania, Go, Brazil
[2] Univ Fed Minas Gerais, Fac Pharm, Belo Horizonte, MG, Brazil
[3] Ezequiel Dias Fdn, Pharmaceut Res & Dev, Rua Conde Pereira Carneiro,80 Gameleira, BR-30510010 Belo Horizonte, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
Nanoparticles; Imiquimod; Skin cancer; Chemopreventive effect; INDUCED SKIN CARCINOGENESIS; BASAL-CELL CARCINOMA; DRUG-DELIVERY; 5-PERCENT CREAM; DOUBLE-BLIND; CANCER; OIL; PENETRATION; VEHICLE; MICE;
D O I
10.1016/j.biopha.2018.04.079
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The chemotherapeutic agent imiquimod (Imq) is used to treat skin cancers, the most common type of human cancer. However, the high incidence of local and systemic side effects associated with its use as well as its low skin permeation impair patient compliance and therapeutic effectiveness To overcome these limitations, nanostructured systems such as nanoparticles can be a promising alternative. Nanoparticles are submicron particles (size less than 1000 nm) with high surface area that facilitates the interaction and cellular uptake by biological membranes. Therefore, the aim of the present work is to evaluate antiangiogenic effect and antitumoral activity of imiquimod-loaded nanoparticles compared to market Imq formulation. Polymeric nanoparticles containing Imq were obtained by the technique of precipitation of preformed polymer. Antiangiogenic activity of the formulations was determined in chicken embryo chorioallantoic membrane (CAM) and its chemopreventive potential was evaluate during multistage DMBA and croton oil model of skin carcinogenesis in mice. Nanoparticles containing Imq presented antiangiogenic activity superior than negative control, placebo dispersion and market Imq (p < 0.05) in the CAM model and also significantly reduced the number and size of papillomas compared to all other groups. These results suggest, therefore, that the obtained delivery system can be an alternative to treat diseases related to vessels formation and also potentially increase cutaneous permeation and efficacy of poor soluble drugs normally used to treat cutaneous diseases.
引用
收藏
页码:1107 / 1114
页数:8
相关论文
共 42 条
  • [1] Topical TLR7 Agonist Imiquimod Can Induce Immune-Mediated Rejection of Skin Metastases in Patients with Breast Cancer
    Adams, Sylvia
    Kozhaya, Lina
    Martiniuk, Frank
    Meng, Tze-Chiang
    Chiriboga, Luis
    Liebes, Leonard
    Hochman, Tsivia
    Shuman, Nicholas
    Axelrod, Deborah
    Speyer, James
    Novik, Yelena
    Tiersten, Amy
    Goldberg, Judith D.
    Formenti, Silvia C.
    Bhardwaj, Nina
    Unutmaz, Derya
    Demaria, Sandra
    [J]. CLINICAL CANCER RESEARCH, 2012, 18 (24) : 6748 - 6757
  • [2] Surgical vs Nonsurgical Treatment of Basal Cell Carcinoma
    Aguayo-Leiva, I. R.
    Rios-Buceta, L.
    Jaen-Olasolo, P.
    [J]. ACTAS DERMO-SIFILIOGRAFICAS, 2010, 101 (08): : 683 - 692
  • [3] Skin Cancer: Epidemiology, Disease Burden, Pathophysiology, Diagnosis, and Therapeutic Approaches
    Apalla, Zoe
    Nashan, Dorothee
    Weller, Richard B.
    Castellsague, Xavier
    [J]. DERMATOLOGY AND THERAPY, 2017, 7 : S5 - S19
  • [4] Formulation and ex vivo evaluation of polymeric nanoparticles for controlled delivery of corticosteroids to the skin and the corneal epithelium
    Balzus, Benjamin
    Sahle, Fitsum Feleke
    Hoenzke, Stefan
    Gerecke, Christian
    Schumacher, Fabian
    Hedtrich, Sarah
    Kleuser, Burkhard
    Bodmeier, Roland
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2017, 115 : 122 - 130
  • [5] Bromelain nanoparticles protect against 7,12-dimethylbenz[a] anthracene induced skin carcinogenesis in mouse model
    Bhatnagar, Priyanka
    Pant, Aditya B.
    Shukla, Yogeshwer
    Chaudhari, Bhushan
    Kumar, Pradeep
    Gupta, Kailash C.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 91 : 35 - 46
  • [6] DLS and zeta potential - What they are and what they are not?
    Bhattacharjee, Sourav
    [J]. JOURNAL OF CONTROLLED RELEASE, 2016, 235 : 337 - 351
  • [7] Formulation and In vitro Characterization of Eudragit® L100 and Eudragit® L100-PLGA Nanoparticles Containing Diclofenac Sodium
    Cetin, Meltem
    Atila, Alptug
    Kadioglu, Yucel
    [J]. AAPS PHARMSCITECH, 2010, 11 (03): : 1250 - 1256
  • [8] dos Santos FK, 2013, CURR NANOSCI, V9, P159
  • [9] El-Nahas A. E., 2017, SILYMARIN LOADED EUD
  • [10] Fessi H., 1989, INT J PHARMACEUT, P55