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Clodronate-liposome-mediated depletion of tumour-associated macrophages: a new and highly effective antiangiogenic therapy approach

British journal of cancer, 2006-08, Vol.95 (3), p.272-281

2006

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Cytotoxic targeting of F9 teratocarcinoma tumours with anti-ED-B fibronectin scFv antibody modified liposomes

British journal of cancer, 2002-07, Vol.87 (1), p.106-112

2002

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In vivo antigen loading and activation of dendritic cells via a liposomal peptide vaccine mediates protective antiviral and anti-tumour immunity

Vaccine, 2000-08, Vol.19 (1), p.23-32

2000

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Lipophilic 1-β-D-arabinofuranosyl cytosine derivatives in liposomal formulations for oral and parenteral antileukemic therapy in the murine L1210 leukemia model

Journal of cancer research and clinical oncology, 1996, Vol.122 (12), p.723-726

1996

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The novel heterodinucleoside dimer 5-FdU-NOAC is a potent cytotoxic drug and a p53-independent inducer of apoptosis in the androgen-independent human prostate cancer cell lines PC-3 and DU-145

The Prostate, 2000-09, Vol.45 (1), p.8-18

2000

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Limited Mycobacterial Infection of the Liver as a Consequence of Its Microanatomical Structure Causing Restriction of Mycobacterial Growth to Professional Phagocytes

Infection and Immunity, 2001-12, Vol.69 (12), p.7922-7926

2001

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Treatment of l1210 murine leukemia with liposome‐incorporated N4‐hexadecyl‐1‐β‐D‐arabinofuranosyl cytosine

International journal of cancer, 1992-05, Vol.51 (3), p.466-469

1992

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Comparative pharmacokinetic and cytotoxic analysis of three different formulations of mitoxantrone in mice

British journal of cancer, 1997, Vol.75 (7), p.986-992

1997

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Cell-cycle arrest and p53-independent induction of apoptosis in vitro by the new anticancer drugs 5-FdUrd-P-FdCydOct and dCydPam-P-FdUrd in DU-145 human prostate cancer cells

Journal of cancer research and clinical oncology, 2000-05, Vol.126 (5), p.247-256

2000

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Pharmacokinetic studies of mitoxantrone and one of its metabolites in serum and urine in patients with advanced breast cancer

European journal of clinical pharmacology, 1998-03, Vol.54 (1), p.83-89

1998

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In vitro Anti-Human Immunodeficiency Virus and Anti-Hepatitis B Virus Activities and Pharmacokinetic Properties of Heterodinucleoside Phosphates Containing AZT or ddC

Antiviral chemistry & chemotherapy, 1998-03, Vol.9 (2), p.117-126

1998

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Synthesis and in vitro anti-HIV activities of amphiphilic heterodinucleoside phosphate derivatives containing the 2',3'-dideoxynucleosides ddC, AZT and ddI

European journal of medicinal chemistry, 1999-04, Vol.34 (4), p.343-352

1999

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Cell cycle-dependent cytotoxicity and induction of apoptosis by liposomal N4-hexadecyl-1-β-D-arabinofuranosylcytosine

British journal of cancer, 1995-11, Vol.72 (5), p.1067-1073

1995

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Cellular pharmacology of a liposomal preparation of N4-hexadecyl-1-β-D-arabinofuranosylcytosine, a lipophilic derivative of 1-β-D-arabinofuranosylcytosine

British journal of cancer, 1995-05, Vol.71 (5), p.957-962

1995

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New lipophilic alkyl/acyl dinucleoside phosphates as derivatives of 3′-azido-3′-deoxythymidine: Inhibition of HIV-1 replication in vitro and antiviral activity against Rauscher leukemia virus infected mice with delayed treatment regimens

Antiviral research, 1994-05, Vol.24 (1), p.79-93

1994

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Pharmacokinetic Properties and Interactions with Blood Components of N4-Hexadecyl-1-β-d-arabinofuranosylcytosine (NHAC) Incorporated into Liposomes

Journal of pharmacy and pharmacology, 1995-04, Vol.47 (4), p.282-288

1995

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Synthesis and in vitro Antiviral Properties of Amphiphilic Dinucleoside Phosphate Derivatives of 2′,3-dideoxycytidine (ddC)

Antiviral chemistry & chemotherapy, 1995-10, Vol.6 (5), p.320-326

1995

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Synthesis, and Some Properties of, Amphiphilic Dinucleoside Phosphate Derivatives of 3′-azido-2′,3′-dideoxythymidine (AZT)

Antiviral chemistry & chemotherapy, 1994-12, Vol.5 (6), p.387-394

1994

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Chromatography of functionalized liposomes and their components

Journal of Chromatography A, 1988-05, Vol.441 (1), p.115-124

1988

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Evaluation of incorporation characteristics of mitoxantrone into unilamellar liposomes and analysis of their pharmacokinetic properties, acute toxicity, and antitumor efficacy

Cancer chemotherapy and pharmacology, 1991-01, Vol.27 (6), p.429-439

1991

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Incorporation of chlorpromazine into bilayer liposomes for protection against microsomal metabolism and liver absorption

European journal of drug metabolism and pharmacokinetics, 1988-04, Vol.13 (2), p.135-141

SCHWENDENER, R. A

1988

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Induction of cell cycle-dependent cytotoxicity and apoptosis by new heterodinucleoside phosphate dimers of 5-fluorodeoxyuridine in PC-3 human prostate cancer cells

Biochemical pharmacology, 2000-12, Vol.60 (12), p.1887-1896

2000

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The preparation of large volumes of homogeneous, sterile liposomes containing various lipophilic cytostatic drugs by the use of a capillary dialyzer

Cancer drug delivery, 1986, Vol.3 (2), p.123-129

SCHWENDENER, R. A

1986

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In vitro activity of liposomal N4octadecyl-1-β-D-arabinofuranosylcytosine (NOAC), a new lipophilic derivative of 1-β-D-arabinofuranocylcytosine on biopsized clonogenic human tumor cells and hematopoietic precursor cells

Investigational new drugs, 2001, Vol.19 (3), p.203-210

2001

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Toxicity of liposomal 3'-5'-O-dipalmitoyl-5-fluoro-2'-deoxyuridine in mice

Anti-cancer drug design, 1998-06, Vol.13 (4), p.291

1998

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Clodronate-liposome-mediated depletion of tumour-associated macrophages: a new and highly effective antiangiogenic therapy approach

Cytotoxic targeting of F9 teratocarcinoma tumours with anti-ED-B fibronectin scFv antibody modified liposomes

In vivo antigen loading and activation of dendritic cells via a liposomal peptide vaccine mediates protective antiviral and anti-tumour immunity

Lipophilic 1-β-D-arabinofuranosyl cytosine derivatives in liposomal formulations for oral and parenteral antileukemic therapy in the murine L1210 leukemia model

The novel heterodinucleoside dimer 5-FdU-NOAC is a potent cytotoxic drug and a p53-independent inducer of apoptosis in the androgen-independent human prostate cancer cell lines PC-3 and DU-145

Limited Mycobacterial Infection of the Liver as a Consequence of Its Microanatomical Structure Causing Restriction of Mycobacterial Growth to Professional Phagocytes

Treatment of l1210 murine leukemia with liposome‐incorporated N4‐hexadecyl‐1‐β‐D‐arabinofuranosyl cytosine

Comparative pharmacokinetic and cytotoxic analysis of three different formulations of mitoxantrone in mice

Cell-cycle arrest and p53-independent induction of apoptosis in vitro by the new anticancer drugs 5-FdUrd-P-FdCydOct and dCydPam-P-FdUrd in DU-145 human prostate cancer cells

Pharmacokinetic studies of mitoxantrone and one of its metabolites in serum and urine in patients with advanced breast cancer

In vitro Anti-Human Immunodeficiency Virus and Anti-Hepatitis B Virus Activities and Pharmacokinetic Properties of Heterodinucleoside Phosphates Containing AZT or ddC

Synthesis and in vitro anti-HIV activities of amphiphilic heterodinucleoside phosphate derivatives containing the 2',3'-dideoxynucleosides ddC, AZT and ddI

Cell cycle-dependent cytotoxicity and induction of apoptosis by liposomal N4-hexadecyl-1-β-D-arabinofuranosylcytosine

Cellular pharmacology of a liposomal preparation of N4-hexadecyl-1-β-D-arabinofuranosylcytosine, a lipophilic derivative of 1-β-D-arabinofuranosylcytosine

New lipophilic alkyl/acyl dinucleoside phosphates as derivatives of 3′-azido-3′-deoxythymidine: Inhibition of HIV-1 replication in vitro and antiviral activity against Rauscher leukemia virus infected mice with delayed treatment regimens

Pharmacokinetic Properties and Interactions with Blood Components of N4-Hexadecyl-1-β-d-arabinofuranosylcytosine (NHAC) Incorporated into Liposomes

Synthesis and in vitro Antiviral Properties of Amphiphilic Dinucleoside Phosphate Derivatives of 2′,3-dideoxycytidine (ddC)

Synthesis, and Some Properties of, Amphiphilic Dinucleoside Phosphate Derivatives of 3′-azido-2′,3′-dideoxythymidine (AZT)

Chromatography of functionalized liposomes and their components

Evaluation of incorporation characteristics of mitoxantrone into unilamellar liposomes and analysis of their pharmacokinetic properties, acute toxicity, and antitumor efficacy

Incorporation of chlorpromazine into bilayer liposomes for protection against microsomal metabolism and liver absorption

Induction of cell cycle-dependent cytotoxicity and apoptosis by new heterodinucleoside phosphate dimers of 5-fluorodeoxyuridine in PC-3 human prostate cancer cells

The preparation of large volumes of homogeneous, sterile liposomes containing various lipophilic cytostatic drugs by the use of a capillary dialyzer

In vitro activity of liposomal N4octadecyl-1-β-D-arabinofuranosylcytosine (NOAC), a new lipophilic derivative of 1-β-D-arabinofuranocylcytosine on biopsized clonogenic human tumor cells and hematopoietic precursor cells

Toxicity of liposomal 3'-5'-O-dipalmitoyl-5-fluoro-2'-deoxyuridine in mice

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