Antitumor Effect of Bleomycin Nanoaerosol in Murine Carcinoma Model

被引:3
作者
Karshieva, Saida S. [1 ]
Babayeva, Gulalek [1 ,2 ]
Pokrovsky, Vadim S. [1 ,2 ,3 ]
Shlyapnikov, Yuri M. [4 ]
Shlyapnikova, Elena A. [4 ]
Bugrova, Anna E. [5 ]
Kononikhin, Alexey S. [6 ]
Nikolaev, Evgeny N. [6 ]
Kanev, Igor L. [4 ]
机构
[1] NN Blokhin Natl Med Res Ctr Oncol, Lab Biochem Pharmacol & Canc Models, Moscow 115478, Russia
[2] Patrice Lumumba Peoples Friendship Univ, Res Inst Mol & Cellular Med, Moscow 117198, Russia
[3] Sirius Univ Sci & Technol, Ctr Genet & Life Sci, Soci 354340, Russia
[4] Russian Acad Sci, Inst Theoret & Expt Biophys, Pushchino 142290, Moscow Region, Russia
[5] Russian Acad Sci, Emanuel Inst Biochem Phys, Moscow 119334, Russia
[6] Skolkovo Inst Sci & Technol, Ctr Life Sci, Moscow 121205, Russia
关键词
lung cancer; nanoaerosol; nanoparticles; bleomycin; pharmacokinetics; drug delivery; SOLID LIPID NANOPARTICLES; PULMONARY-FIBROSIS; INHALATION DELIVERY; COPOLYMER MICELLES; LUNG; GENERATION; DRUG; RAT; INTRATRACHEAL; NANOMEDICINE;
D O I
10.3390/molecules28104157
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bleomycin, which is widely used as an antitumor agent, possesses serious adverse effects such as pulmonary toxicity. Local nanoaerosol deposition for lung cancer treatment is a promising alternative to drug delivery to lung lesions. The aim of this work is to test the hypothesis that bleomycin nanoaerosol can be effectively used to treat multiple lung metastases. To obtain bleomycin nanoaerosol, an aerosol generator based on electrospray of a solution of a nonvolatile substance with gas-phase neutralization of charged aerosol particles was used. Lung metastases in murine Lewis lung carcinoma and B16 melanoma animal models were counted. The effect of inhaled bleomycin nanoparticles on the number and volume of metastases, as well as pulmonary side effects, was investigated. Using a mouse exposure chamber, the dose-dependent effect of inhaled bleomycin on tumor volume was evaluated in comparison with intraperitoneal administration. Bleomycin nanoaerosol reduced the volume of metastases and produced a higher antitumor effect at much lower doses. It has been established that long-term exposure to nanoaerosol with a low dose of bleomycin is capable of suppressing cancer cell growth. The treatment was well tolerated. In the lungs, minor changes were found in the form of focal-diffuse infiltration of the lung parenchyma.
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页数:15
相关论文
共 53 条
[1]   Nanotechnology-based inhalation treatments for lung cancer: state of the art [J].
Ahmad, Javed ;
Akhter, Sohail ;
Rizwanullah, Md ;
Amin, Saima ;
Rahman, Mahfoozur ;
Ahmad, Mohammad Zaki ;
Rizvi, Moshahid Alam ;
Kamal, Mohammad A. ;
Ahmad, Farhan Jalees .
NANOTECHNOLOGY SCIENCE AND APPLICATIONS, 2015, 8 :55-66
[2]   Prospective of extracellular matrix and drug correlations in disease management [J].
Ahmad, Varish .
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2021, 16 (02) :147-160
[3]   A MULTIPLE-PATH MODEL OF PARTICLE DEPOSITION IN THE RAT LUNG [J].
ANJILVEL, S ;
ASGHARIAN, B .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1995, 28 (01) :41-50
[4]   AN INVESTIGATION OF POSSIBLE MODELS FOR THE PRODUCTION OF PROGRESSIVE PULMONARY FIBROSIS IN THE RAT - THE EFFECTS OF REPEATED INTRATRACHEAL INSTILLATION OF BLEOMYCIN [J].
BROWN, RFR ;
DRAWBAUGH, RB ;
MARRS, TC .
TOXICOLOGY, 1988, 51 (01) :101-110
[5]   Death by bleomycin pulmonary toxicity in ovarian dysgerminoma with pathologic complete response to chemotherapy. A case report [J].
Calzas Rodriguez, Julia ;
Juarez Morales, Maria del Carmen ;
Racionero Casero, Miguel Angel .
RESPIRATORY MEDICINE CASE REPORTS, 2016, 18 :48-50
[6]  
Curtis John, 2006, Toxicol Rev, V25, P245, DOI 10.2165/00139709-200625040-00005
[7]   TGF-β-induced fibrosis and SMAD signaling:: oligo decoys as natural therapeutics for inhibition of tissue fibrosis and scarring [J].
Cutroneo, Kenneth R. .
WOUND REPAIR AND REGENERATION, 2007, 15 :S54-S60
[8]  
DAVY M, 1985, CANCER CHEMOTH PHARM, V14, P274
[9]  
El-Maradny H., 2022, DRUG DELIV LETT, V12, P258, DOI [10.2174/2210303112666220831100748, DOI 10.2174/2210303112666220831100748]
[10]   What do we (need to) know about the kinetic properties of nanoparticles in the body? [J].
Hagens, Werner I. ;
Oomen, Agnes G. ;
de Jong, Wim H. ;
Cassee, Flemming R. ;
Sips, Adrienne J. A. M. .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2007, 49 (03) :217-229